Linked Data
dbSNP Id:
rs121908926
ExAC:
9:139571055 G / A
gnomAD v2:
9-139571055-G-A
gnomAD v4:
9-136676603-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.136676603G>A , CM000671.2:g.136676603G>A | GRCh38 |
| NC_000009.11:g.139571055G>A , CM000671.1:g.139571055G>A | GRCh37 |
| NC_000009.10:g.138690876G>A | NCBI36 |
| NG_008090.1:g.15857C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000371696.7:c.570C>T MANE Select | ENSP00000360761.2:p.Tyr190= | |
| ENST00000371694.7:c.492+358C>T | ENSP00000360759.3:n.492+358C>T | |
| ENST00000371696.6:c.570C>T | ENSP00000360761.2:p.Tyr190= | |
| ENST00000472820.1:n.498C>T | ||
| ENST00000538402.1:c.570C>T | ENSP00000438919.1:p.Tyr190= | |
| NM_001012727.1:c.492+358C>T | NP_001012745.1:n.492+358C>T | |
| NM_006412.3:c.570C>T | NP_006403.2:p.Tyr190= | |
| NM_006412.4:c.570C>T MANE Select | NP_006403.2:p.Tyr190= | |
| NM_001012727.2:c.492+358C>T | NP_001012745.1:n.492+358C>T |