Linked Data
dbSNP Id:
rs748506070
ExAC:
7:150647497 G / T
gnomAD v2:
7-150647497-G-T
gnomAD v4:
7-150950409-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.150950409G>T , CM000669.2:g.150950409G>T | GRCh38 |
| NC_000007.13:g.150647497G>T , CM000669.1:g.150647497G>T | GRCh37 |
| NC_000007.12:g.150278430G>T | NCBI36 |
| NG_008916.1:g.32518C>A , LRG_288:g.32518C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000461280.2:n.1455C>A | ||
| ENST00000684241.1:n.2990C>A | ||
| ENST00000262186.10:c.2157C>A MANE Select | ENSP00000262186.5:p.Gly719= | |
| ENST00000330883.9:c.1137C>A | ENSP00000328531.4:p.Gly379= | |
| ENST00000262186.9:c.2157C>A | ENSP00000262186.5:p.Gly719= | |
| ENST00000330883.8:c.1137C>A | ENSP00000328531.4:p.Gly379= | |
| ENST00000430723.4:c.1809C>A | ENSP00000387657.4:p.Gly603= | |
| ENST00000461280.1:n.1444C>A | ||
| ENST00000473610.5:n.1789C>A | ||
| ENST00000532957.5:n.2380C>A | ||
| NM_000238.3:c.2157C>A , LRG_288t1:c.2157C>A | NP_000229.1:p.Gly719= | |
| NM_001204798.1:c.1137C>A | NP_001191727.1:p.Gly379= | |
| NM_172056.2:c.2157C>A , LRG_288t2:c.2157C>A | NP_742053.1:p.Gly719= | |
| NM_172057.2:c.1137C>A , LRG_288t3:c.1137C>A | NP_742054.1:p.Gly379= | |
| XM_011516185.1:c.1857C>A | XP_011514487.1:p.Gly619= | |
| XM_011516186.1:c.2157C>A | XP_011514488.1:p.Gly719= | |
| XM_011516185.2:c.1857C>A | XP_011514487.1:p.Gly619= | |
| XM_011516186.3:c.2157C>A | XP_011514488.1:p.Gly719= | |
| XM_017012195.1:c.2007C>A | XP_016867684.1:p.Gly669= | |
| XM_017012196.1:c.1980C>A | XP_016867685.1:p.Gly660= | |
| NM_000238.4:c.2157C>A MANE Select | NP_000229.1:p.Gly719= | |
| NM_001204798.2:c.1137C>A | NP_001191727.1:p.Gly379= | |
| NM_172057.3:c.1137C>A | NP_742054.1:p.Gly379= |