Linked Data
dbSNP Id:
rs776268465
gnomAD v2:
19-7184386-G-T
gnomAD v3:
19-7184375-G-T
gnomAD v4:
19-7184375-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.7184375G>T , CM000681.2:g.7184375G>T | GRCh38 |
| NC_000019.9:g.7184386G>T , CM000681.1:g.7184386G>T | GRCh37 |
| NC_000019.8:g.7135386G>T | NCBI36 |
| NG_008852.2:g.114626C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000302850.10:c.915C>A MANE Select | ENSP00000303830.4:p.Val305= | |
| ENST00000302850.9:c.915C>A | ENSP00000303830.4:p.Val305= | |
| ENST00000341500.9:c.915C>A | ENSP00000342838.4:p.Val305= | |
| ENST00000598216.1:n.890C>A | ||
| NM_000208.2:c.915C>A | NP_000199.2:p.Val305= | |
| NM_000208.3:c.915C>A | NP_000199.2:p.Val305= | |
| NM_001079817.1:c.915C>A | NP_001073285.1:p.Val305= | |
| NM_001079817.2:c.915C>A | NP_001073285.1:p.Val305= | |
| XM_011527988.1:c.993C>A | XP_011526290.1:p.Val331= | |
| XM_011527989.1:c.993C>A | XP_011526291.1:p.Val331= | |
| XM_011527988.2:c.915C>A | XP_011526290.2:p.Val305= | |
| XM_011527989.3:c.915C>A | XP_011526291.2:p.Val305= | |
| NM_000208.4:c.915C>A MANE Select | NP_000199.2:p.Val305= | |
| NM_001079817.3:c.915C>A | NP_001073285.1:p.Val305= |