Linked Data
dbSNP Id:
rs763064903
ExAC:
16:3779081 C / T
gnomAD v2:
16-3779081-C-T
gnomAD v3:
16-3729080-C-T
gnomAD v4:
16-3729080-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.3729080C>T , CM000678.2:g.3729080C>T | GRCh38 |
| NC_000016.9:g.3779081C>T , CM000678.1:g.3779081C>T | GRCh37 |
| NC_000016.8:g.3719082C>T | NCBI36 |
| NG_009873.1:g.156041G>A | |
| NG_009873.2:g.156634G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000262367.10:c.5967G>A MANE Select | ENSP00000262367.5:p.Gly1989= | |
| ENST00000262367.9:c.5967G>A | ENSP00000262367.5:p.Gly1989= | |
| ENST00000382070.7:c.5853G>A | ENSP00000371502.3:p.Gly1951= | |
| NM_001079846.1:c.5853G>A | NP_001073315.1:p.Gly1951= | |
| NM_004380.2:c.5967G>A | NP_004371.2:p.Gly1989= | |
| XM_005255124.3:c.5922G>A | XP_005255181.1:p.Gly1974= | |
| XM_005255125.3:c.5550G>A | XP_005255182.1:p.Gly1850= | |
| XM_006720848.2:c.5706G>A | XP_006720911.1:p.Gly1902= | |
| XM_011522380.1:c.5913G>A | XP_011520682.1:p.Gly1971= | |
| XM_011522381.1:c.5214G>A | XP_011520683.1:p.Gly1738= | |
| XM_005255124.4:c.5922G>A | XP_005255181.1:p.Gly1974= | |
| XM_005255125.4:c.5550G>A | XP_005255182.1:p.Gly1850= | |
| XM_006720848.3:c.5706G>A | XP_006720911.1:p.Gly1902= | |
| XM_011522381.2:c.5214G>A | XP_011520683.1:p.Gly1738= | |
| XM_017022944.1:c.5961G>A | XP_016878433.1:p.Gly1987= | |
| NM_004380.3:c.5967G>A MANE Select | NP_004371.2:p.Gly1989= |