Linked Data
dbSNP Id:
rs890149316
gnomAD v2:
19-7184257-G-A
gnomAD v3:
19-7184246-G-A
gnomAD v4:
19-7184246-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.7184246G>A , CM000681.2:g.7184246G>A | GRCh38 |
| NC_000019.9:g.7184257G>A , CM000681.1:g.7184257G>A | GRCh37 |
| NC_000019.8:g.7135257G>A | NCBI36 |
| NG_008852.2:g.114755C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000302850.10:c.974+70C>T MANE Select | ENSP00000303830.4:n.974+70C>T | |
| ENST00000302850.9:c.974+70C>T | ENSP00000303830.4:n.974+70C>T | |
| ENST00000341500.9:c.974+70C>T | ENSP00000342838.4:n.974+70C>T | |
| ENST00000598216.1:n.949+70C>T | ||
| NM_000208.2:c.974+70C>T | NP_000199.2:n.974+70C>T | |
| NM_000208.3:c.974+70C>T | NP_000199.2:n.974+70C>T | |
| NM_001079817.1:c.974+70C>T | NP_001073285.1:n.974+70C>T | |
| NM_001079817.2:c.974+70C>T | NP_001073285.1:n.974+70C>T | |
| XM_011527988.1:c.1052+70C>T | XP_011526290.1:n.1052+70C>T | |
| XM_011527989.1:c.1052+70C>T | XP_011526291.1:n.1052+70C>T | |
| XM_011527988.2:c.974+70C>T | XP_011526290.2:n.974+70C>T | |
| XM_011527989.3:c.974+70C>T | XP_011526291.2:n.974+70C>T | |
| NM_000208.4:c.974+70C>T MANE Select | NP_000199.2:n.974+70C>T | |
| NM_001079817.3:c.974+70C>T | NP_001073285.1:n.974+70C>T |