Linked Data
dbSNP Id:
rs778168390
ExAC:
12:48526658 C / T
gnomAD v2:
12-48526658-C-T
gnomAD v4:
12-48132875-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.48132875C>T , CM000674.2:g.48132875C>T | GRCh38 |
| NC_000012.11:g.48526658C>T , CM000674.1:g.48526658C>T | GRCh37 |
| NC_000012.10:g.46812925C>T | NCBI36 |
| NG_016199.1:g.32003C>T | |
| NG_016199.2:g.32623C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000550257.7:c.467C>T | ENSP00000447997.3:p.Thr156Met | |
| ENST00000340802.12:c.458C>T | ENSP00000345771.6:p.Thr153Met | |
| ENST00000359794.11:c.245C>T MANE Select | ENSP00000352842.5:p.Thr82Met | |
| ENST00000549941.7:c.245C>T | ENSP00000446829.3:p.Thr82Met | |
| ENST00000550345.6:c.245C>T | ENSP00000450369.2:p.Thr82Met | |
| ENST00000550924.6:c.245C>T | ENSP00000446945.2:p.Thr82Met | |
| ENST00000551339.6:c.245C>T | ENSP00000448253.2:p.Thr82Met | |
| ENST00000642730.1:c.554C>T | ENSP00000496597.1:p.Thr185Met | |
| ENST00000312352.11:c.245C>T | ENSP00000309438.7:p.Thr82Met | |
| ENST00000340802.10:c.458C>T | ENSP00000345771.6:p.Thr153Met | |
| ENST00000359794.9:c.245C>T | ENSP00000352842.5:p.Thr82Met | |
| ENST00000546465.1:c.86-7896C>T | ENSP00000446519.1:n.86-7896C>T | |
| ENST00000546964.5:n.317C>T | ||
| ENST00000547581.5:c.*261C>T | ENSP00000447992.1:n.*261C>T | |
| ENST00000547587.5:c.245C>T | ENSP00000449426.1:p.Thr82Met | |
| ENST00000548345.5:c.245C>T | ENSP00000449269.1:p.Thr82Met | |
| ENST00000549003.5:c.245C>T | ENSP00000449835.1:p.Thr82Met | |
| ENST00000549022.5:c.245C>T | ENSP00000446805.1:p.Thr82Met | |
| ENST00000549941.5:c.344C>T | ENSP00000446829.1:p.Thr115Met | |
| ENST00000550345.5:c.245C>T | ENSP00000450369.1:p.Thr82Met | |
| ENST00000550924.5:c.245C>T | ENSP00000446945.1:p.Thr82Met | |
| ENST00000551339.5:c.245C>T | ENSP00000448253.1:p.Thr82Met | |
| ENST00000551485.5:c.*129C>T | ENSP00000448315.1:n.*129C>T | |
| ENST00000551804.5:c.245C>T | ENSP00000448177.1:p.Thr82Met | |
| ENST00000552989.5:c.86-1364C>T | ENSP00000447774.1:n.86-1364C>T | |
| NM_000289.5:c.245C>T | NP_000280.1:p.Thr82Met | |
| NM_001166686.1:c.458C>T | NP_001160158.1:p.Thr153Met | |
| NM_001166687.1:c.245C>T | NP_001160159.1:p.Thr82Met | |
| NM_001166688.1:c.245C>T | NP_001160160.1:p.Thr82Met | |
| XM_005268974.1:c.554C>T | XP_005269031.1:p.Thr185Met | |
| XM_005268975.1:c.554C>T | XP_005269032.1:p.Thr185Met | |
| XM_005268976.2:c.554C>T | XP_005269033.1:p.Thr185Met | |
| XM_005268977.1:c.458C>T | XP_005269034.1:p.Thr153Met | |
| XM_005268978.2:c.458C>T | XP_005269035.1:p.Thr153Met | |
| XM_005268979.1:c.458C>T | XP_005269036.1:p.Thr153Met | |
| XM_011538487.1:c.554C>T | XP_011536789.1:p.Thr185Met | |
| XM_011538488.1:c.245C>T | XP_011536790.1:p.Thr82Met | |
| NM_000289.6:c.245C>T MANE Select | NP_000280.1:p.Thr82Met | |
| NM_001166686.2:c.458C>T | NP_001160158.1:p.Thr153Met | |
| NM_001354735.1:c.554C>T | NP_001341664.1:p.Thr185Met | |
| NM_001354736.1:c.554C>T | NP_001341665.1:p.Thr185Met | |
| NM_001354737.1:c.458C>T | NP_001341666.1:p.Thr153Met | |
| NM_001354738.1:c.458C>T | NP_001341667.1:p.Thr153Met | |
| NM_001354739.1:c.458C>T | NP_001341668.1:p.Thr153Met | |
| NM_001354740.1:c.389C>T | NP_001341669.1:p.Thr130Met | |
| NM_001354741.1:c.269C>T | NP_001341670.1:p.Thr90Met | |
| NM_001354742.1:c.245C>T | NP_001341671.1:p.Thr82Met | |
| NM_001354743.1:c.245C>T | NP_001341672.1:p.Thr82Met | |
| NM_001354744.1:c.245C>T | NP_001341673.1:p.Thr82Met | |
| NM_001354745.1:c.158C>T | NP_001341674.1:p.Thr53Met | |
| NM_001354746.1:c.245C>T | NP_001341675.1:p.Thr82Met | |
| NM_001354747.1:c.95C>T | NP_001341676.1:p.Thr32Met | |
| NM_001354748.1:c.95C>T | NP_001341677.1:p.Thr32Met | |
| NM_001363619.1:c.245C>T | NP_001350548.1:p.Thr82Met | |
| NR_148954.1:n.430C>T | ||
| NR_148955.1:n.1066C>T | ||
| NR_148956.1:n.356C>T | ||
| NR_148957.1:n.430C>T | ||
| NR_148958.1:n.430C>T | ||
| NR_148959.1:n.356C>T | ||
| XM_005268976.3:c.554C>T | XP_005269033.1:p.Thr185Met | |
| XM_017019469.1:c.458C>T | XP_016874958.1:p.Thr153Met | |
| XM_024449020.1:c.467C>T | XP_024304788.1:p.Thr156Met | |
| XM_024449021.1:c.344C>T | XP_024304789.1:p.Thr115Met | |
| XM_024449022.1:c.245C>T | XP_024304790.1:p.Thr82Met | |
| NM_001166687.2:c.245C>T | NP_001160159.1:p.Thr82Met | |
| NM_001166688.2:c.245C>T | NP_001160160.1:p.Thr82Met | |
| NM_001354741.2:c.269C>T | NP_001341670.1:p.Thr90Met | |
| NM_001354742.2:c.245C>T | NP_001341671.1:p.Thr82Met | |
| NM_001354743.2:c.245C>T | NP_001341672.1:p.Thr82Met | |
| NM_001354744.2:c.245C>T | NP_001341673.1:p.Thr82Met | |
| NM_001354745.2:c.158C>T | NP_001341674.1:p.Thr53Met | |
| NM_001354746.2:c.245C>T | NP_001341675.1:p.Thr82Met | |
| NM_001354747.2:c.95C>T | NP_001341676.1:p.Thr32Met | |
| NM_001354748.2:c.95C>T | NP_001341677.1:p.Thr32Met | |
| NM_001363619.2:c.245C>T | NP_001350548.1:p.Thr82Met | |
| NR_148954.2:n.296C>T | ||
| NR_148956.2:n.222C>T | ||
| NR_148957.2:n.296C>T | ||
| NR_148958.2:n.296C>T | ||
| NR_148959.2:n.222C>T |