Linked Data
dbSNP Id:
rs758263277
ExAC:
3:119530473 T / G
gnomAD v2:
3-119530473-T-G
gnomAD v4:
3-119811626-T-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.119811626T>G , CM000665.2:g.119811626T>G | GRCh38 |
| NC_000003.11:g.119530473T>G , CM000665.1:g.119530473T>G | GRCh37 |
| NC_000003.10:g.121013163T>G | NCBI36 |
| NG_011856.1:g.36143T>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000393716.8:c.419T>G MANE Select | ENSP00000377319.3:p.Val140Gly | |
| ENST00000466380.6:c.419T>G | ENSP00000420297.2:p.Val140Gly | |
| ENST00000337940.4:c.536T>G | ENSP00000336528.4:p.Val179Gly | |
| ENST00000393716.6:c.419T>G | ENSP00000377319.2:p.Val140Gly | |
| ENST00000466380.5:c.419T>G | ENSP00000420297.1:p.Val140Gly | |
| ENST00000493757.1:n.551T>G | ||
| NM_003889.3:c.419T>G | NP_003880.3:p.Val140Gly | |
| NM_022002.2:c.536T>G | NP_071285.1:p.Val179Gly | |
| NM_033013.2:c.419T>G | NP_148934.1:p.Val140Gly | |
| NM_003889.4:c.419T>G MANE Select | NP_003880.3:p.Val140Gly | |
| NM_022002.3:c.536T>G | NP_071285.1:p.Val179Gly | |
| NM_033013.3:c.419T>G | NP_148934.1:p.Val140Gly |