Linked Data
dbSNP Id:
rs10426094
gnomAD v2:
19-7205240-C-T
gnomAD v3:
19-7205229-C-T
gnomAD v4:
19-7205229-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.7205229C>T , CM000681.2:g.7205229C>T | GRCh38 |
| NC_000019.9:g.7205240C>T , CM000681.1:g.7205240C>T | GRCh37 |
| NC_000019.8:g.7156240C>T | NCBI36 |
| NG_008852.2:g.93772G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000302850.10:c.653-20592G>A MANE Select | ENSP00000303830.4:n.653-20592G>A | |
| ENST00000302850.9:c.653-20592G>A | ENSP00000303830.4:n.653-20592G>A | |
| ENST00000341500.9:c.653-20592G>A | ENSP00000342838.4:n.653-20592G>A | |
| ENST00000598216.1:n.628-20592G>A | ||
| NM_000208.2:c.653-20592G>A | NP_000199.2:n.653-20592G>A | |
| NM_000208.3:c.653-20592G>A | NP_000199.2:n.653-20592G>A | |
| NM_001079817.1:c.653-20592G>A | NP_001073285.1:n.653-20592G>A | |
| NM_001079817.2:c.653-20592G>A | NP_001073285.1:n.653-20592G>A | |
| XM_011527988.1:c.731-20592G>A | XP_011526290.1:n.731-20592G>A | |
| XM_011527989.1:c.731-20592G>A | XP_011526291.1:n.731-20592G>A | |
| XM_011527988.2:c.653-20592G>A | XP_011526290.2:n.653-20592G>A | |
| XM_011527989.3:c.653-20592G>A | XP_011526291.2:n.653-20592G>A | |
| NM_000208.4:c.653-20592G>A MANE Select | NP_000199.2:n.653-20592G>A | |
| NM_001079817.3:c.653-20592G>A | NP_001073285.1:n.653-20592G>A |