Linked Data
dbSNP Id:
rs1473421615
gnomAD v2:
19-7117004-G-A
gnomAD v3:
19-7116993-G-A
gnomAD v4:
19-7116993-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.7116993G>A , CM000681.2:g.7116993G>A | GRCh38 |
| NC_000019.9:g.7117004G>A , CM000681.1:g.7117004G>A | GRCh37 |
| NC_000019.8:g.7068004G>A | NCBI36 |
| NG_008852.2:g.182008C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000302850.10:c.*63C>T MANE Select | ENSP00000303830.4:n.*63C>T | |
| ENST00000302850.9:c.*63C>T | ENSP00000303830.4:n.*63C>T | |
| ENST00000341500.9:c.*63C>T | ENSP00000342838.4:n.*63C>T | |
| NM_000208.2:c.*63C>T | NP_000199.2:n.*63C>T | |
| NM_000208.3:c.*63C>T | NP_000199.2:n.*63C>T | |
| NM_001079817.1:c.*63C>T | NP_001073285.1:n.*63C>T | |
| NM_001079817.2:c.*63C>T | NP_001073285.1:n.*63C>T | |
| XM_011527988.1:c.*63C>T | XP_011526290.1:n.*63C>T | |
| XM_011527989.1:c.*63C>T | XP_011526291.1:n.*63C>T | |
| XM_011527988.2:c.*63C>T | XP_011526290.2:n.*63C>T | |
| XM_011527989.3:c.*63C>T | XP_011526291.2:n.*63C>T | |
| NM_000208.4:c.*63C>T MANE Select | NP_000199.2:n.*63C>T | |
| NM_001079817.3:c.*63C>T | NP_001073285.1:n.*63C>T |