Linked Data
dbSNP Id:
rs760446454
ExAC:
19:7132266 C / A
gnomAD v2:
19-7132266-C-A
gnomAD v4:
19-7132255-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.7132255C>A , CM000681.2:g.7132255C>A | GRCh38 |
| NC_000019.9:g.7132266C>A , CM000681.1:g.7132266C>A | GRCh37 |
| NC_000019.8:g.7083266C>A | NCBI36 |
| NG_008852.2:g.166746G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000302850.10:c.2745G>T MANE Select | ENSP00000303830.4:p.Gly915= | |
| ENST00000302850.9:c.2745G>T | ENSP00000303830.4:p.Gly915= | |
| ENST00000341500.9:c.2709G>T | ENSP00000342838.4:p.Gly903= | |
| NM_000208.2:c.2745G>T | NP_000199.2:p.Gly915= | |
| NM_000208.3:c.2745G>T | NP_000199.2:p.Gly915= | |
| NM_001079817.1:c.2709G>T | NP_001073285.1:p.Gly903= | |
| NM_001079817.2:c.2709G>T | NP_001073285.1:p.Gly903= | |
| XM_011527988.1:c.2823G>T | XP_011526290.1:p.Gly941= | |
| XM_011527989.1:c.2787G>T | XP_011526291.1:p.Gly929= | |
| XM_011527988.2:c.2745G>T | XP_011526290.2:p.Gly915= | |
| XM_011527989.3:c.2709G>T | XP_011526291.2:p.Gly903= | |
| NM_000208.4:c.2745G>T MANE Select | NP_000199.2:p.Gly915= | |
| NM_001079817.3:c.2709G>T | NP_001073285.1:p.Gly903= |