Linked Data
ClinVar Variation Id:
255761
dbSNP Id:
rs11552507
ExAC:
12:48526719 C / T
gnomAD v2:
12-48526719-C-T
gnomAD v3:
12-48132936-C-T
gnomAD v4:
12-48132936-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.48132936C>T , CM000674.2:g.48132936C>T | GRCh38 |
| NC_000012.11:g.48526719C>T , CM000674.1:g.48526719C>T | GRCh37 |
| NC_000012.10:g.46812986C>T | NCBI36 |
| NG_016199.1:g.32064C>T | |
| NG_016199.2:g.32684C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000550257.7:c.528C>T | ENSP00000447997.3:p.Ala176= | |
| ENST00000340802.12:c.519C>T | ENSP00000345771.6:p.Ala173= | |
| ENST00000359794.11:c.306C>T MANE Select | ENSP00000352842.5:p.Ala102= | |
| ENST00000549941.7:c.306C>T | ENSP00000446829.3:p.Ala102= | |
| ENST00000550345.6:c.306C>T | ENSP00000450369.2:p.Ala102= | |
| ENST00000550924.6:c.306C>T | ENSP00000446945.2:p.Ala102= | |
| ENST00000551339.6:c.306C>T | ENSP00000448253.2:p.Ala102= | |
| ENST00000642730.1:c.615C>T | ENSP00000496597.1:p.Ala205= | |
| ENST00000312352.11:c.306C>T | ENSP00000309438.7:p.Ala102= | |
| ENST00000340802.10:c.519C>T | ENSP00000345771.6:p.Ala173= | |
| ENST00000359794.9:c.306C>T | ENSP00000352842.5:p.Ala102= | |
| ENST00000546465.1:c.86-7835C>T | ENSP00000446519.1:n.86-7835C>T | |
| ENST00000546964.5:n.378C>T | ||
| ENST00000547581.5:c.*322C>T | ENSP00000447992.1:n.*322C>T | |
| ENST00000547587.5:c.306C>T | ENSP00000449426.1:p.Ala102= | |
| ENST00000548345.5:c.306C>T | ENSP00000449269.1:p.Ala102= | |
| ENST00000549003.5:c.306C>T | ENSP00000449835.1:p.Ala102= | |
| ENST00000549022.5:c.306C>T | ENSP00000446805.1:p.Ala102= | |
| ENST00000549941.5:c.405C>T | ENSP00000446829.1:p.Ala135= | |
| ENST00000550345.5:c.306C>T | ENSP00000450369.1:p.Ala102= | |
| ENST00000551339.5:c.306C>T | ENSP00000448253.1:p.Ala102= | |
| ENST00000551485.5:c.*190C>T | ENSP00000448315.1:n.*190C>T | |
| ENST00000551804.5:c.306C>T | ENSP00000448177.1:p.Ala102= | |
| ENST00000552989.5:c.86-1303C>T | ENSP00000447774.1:n.86-1303C>T | |
| NM_000289.5:c.306C>T | NP_000280.1:p.Ala102= | |
| NM_001166686.1:c.519C>T | NP_001160158.1:p.Ala173= | |
| NM_001166687.1:c.306C>T | NP_001160159.1:p.Ala102= | |
| NM_001166688.1:c.306C>T | NP_001160160.1:p.Ala102= | |
| XM_005268974.1:c.615C>T | XP_005269031.1:p.Ala205= | |
| XM_005268975.1:c.615C>T | XP_005269032.1:p.Ala205= | |
| XM_005268976.2:c.615C>T | XP_005269033.1:p.Ala205= | |
| XM_005268977.1:c.519C>T | XP_005269034.1:p.Ala173= | |
| XM_005268978.2:c.519C>T | XP_005269035.1:p.Ala173= | |
| XM_005268979.1:c.519C>T | XP_005269036.1:p.Ala173= | |
| XM_011538487.1:c.615C>T | XP_011536789.1:p.Ala205= | |
| XM_011538488.1:c.306C>T | XP_011536790.1:p.Ala102= | |
| NM_000289.6:c.306C>T MANE Select | NP_000280.1:p.Ala102= | |
| NM_001166686.2:c.519C>T | NP_001160158.1:p.Ala173= | |
| NM_001354735.1:c.615C>T | NP_001341664.1:p.Ala205= | |
| NM_001354736.1:c.615C>T | NP_001341665.1:p.Ala205= | |
| NM_001354737.1:c.519C>T | NP_001341666.1:p.Ala173= | |
| NM_001354738.1:c.519C>T | NP_001341667.1:p.Ala173= | |
| NM_001354739.1:c.519C>T | NP_001341668.1:p.Ala173= | |
| NM_001354740.1:c.450C>T | NP_001341669.1:p.Ala150= | |
| NM_001354741.1:c.330C>T | NP_001341670.1:p.Ala110= | |
| NM_001354742.1:c.306C>T | NP_001341671.1:p.Ala102= | |
| NM_001354743.1:c.306C>T | NP_001341672.1:p.Ala102= | |
| NM_001354744.1:c.306C>T | NP_001341673.1:p.Ala102= | |
| NM_001354745.1:c.219C>T | NP_001341674.1:p.Ala73= | |
| NM_001354746.1:c.306C>T | NP_001341675.1:p.Ala102= | |
| NM_001354747.1:c.156C>T | NP_001341676.1:p.Ala52= | |
| NM_001354748.1:c.156C>T | NP_001341677.1:p.Ala52= | |
| NM_001363619.1:c.306C>T | NP_001350548.1:p.Ala102= | |
| NR_148954.1:n.491C>T | ||
| NR_148955.1:n.1127C>T | ||
| NR_148956.1:n.417C>T | ||
| NR_148957.1:n.491C>T | ||
| NR_148958.1:n.491C>T | ||
| NR_148959.1:n.417C>T | ||
| XM_005268976.3:c.615C>T | XP_005269033.1:p.Ala205= | |
| XM_017019469.1:c.519C>T | XP_016874958.1:p.Ala173= | |
| XM_024449020.1:c.528C>T | XP_024304788.1:p.Ala176= | |
| XM_024449021.1:c.405C>T | XP_024304789.1:p.Ala135= | |
| XM_024449022.1:c.306C>T | XP_024304790.1:p.Ala102= | |
| NM_001166687.2:c.306C>T | NP_001160159.1:p.Ala102= | |
| NM_001166688.2:c.306C>T | NP_001160160.1:p.Ala102= | |
| NM_001354741.2:c.330C>T | NP_001341670.1:p.Ala110= | |
| NM_001354742.2:c.306C>T | NP_001341671.1:p.Ala102= | |
| NM_001354743.2:c.306C>T | NP_001341672.1:p.Ala102= | |
| NM_001354744.2:c.306C>T | NP_001341673.1:p.Ala102= | |
| NM_001354745.2:c.219C>T | NP_001341674.1:p.Ala73= | |
| NM_001354746.2:c.306C>T | NP_001341675.1:p.Ala102= | |
| NM_001354747.2:c.156C>T | NP_001341676.1:p.Ala52= | |
| NM_001354748.2:c.156C>T | NP_001341677.1:p.Ala52= | |
| NM_001363619.2:c.306C>T | NP_001350548.1:p.Ala102= | |
| NR_148954.2:n.357C>T | ||
| NR_148956.2:n.283C>T | ||
| NR_148957.2:n.357C>T | ||
| NR_148958.2:n.357C>T | ||
| NR_148959.2:n.283C>T |