Linked Data
ClinVar Variation Id:
220202
dbSNP Id:
rs41314375
ExAC:
7:150648672 G / A
gnomAD v2:
7-150648672-G-A
gnomAD v3:
7-150951584-G-A
gnomAD v4:
7-150951584-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.150951584G>A , CM000669.2:g.150951584G>A | GRCh38 |
| NC_000007.13:g.150648672G>A , CM000669.1:g.150648672G>A | GRCh37 |
| NC_000007.12:g.150279605G>A | NCBI36 |
| NG_008916.1:g.31343C>T , LRG_288:g.31343C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000461280.2:n.1107C>T | ||
| ENST00000684241.1:n.2642C>T | ||
| ENST00000262186.10:c.1809C>T MANE Select | ENSP00000262186.5:p.Gly603= | |
| ENST00000330883.9:c.789C>T | ENSP00000328531.4:p.Gly263= | |
| ENST00000262186.9:c.1809C>T | ENSP00000262186.5:p.Gly603= | |
| ENST00000330883.8:c.789C>T | ENSP00000328531.4:p.Gly263= | |
| ENST00000430723.4:c.1461C>T | ENSP00000387657.4:p.Gly487= | |
| ENST00000461280.1:n.1096C>T | ||
| ENST00000473610.5:n.1114C>T | ||
| ENST00000532957.5:n.2032C>T | ||
| NM_000238.3:c.1809C>T , LRG_288t1:c.1809C>T | NP_000229.1:p.Gly603= | |
| NM_001204798.1:c.789C>T | NP_001191727.1:p.Gly263= | |
| NM_172056.2:c.1809C>T , LRG_288t2:c.1809C>T | NP_742053.1:p.Gly603= | |
| NM_172057.2:c.789C>T , LRG_288t3:c.789C>T | NP_742054.1:p.Gly263= | |
| XM_011516185.1:c.1509C>T | XP_011514487.1:p.Gly503= | |
| XM_011516186.1:c.1809C>T | XP_011514488.1:p.Gly603= | |
| XM_011516185.2:c.1509C>T | XP_011514487.1:p.Gly503= | |
| XM_011516186.3:c.1809C>T | XP_011514488.1:p.Gly603= | |
| XM_017012195.1:c.1659C>T | XP_016867684.1:p.Gly553= | |
| XM_017012196.1:c.1632C>T | XP_016867685.1:p.Gly544= | |
| NM_000238.4:c.1809C>T MANE Select | NP_000229.1:p.Gly603= | |
| NM_001204798.2:c.789C>T | NP_001191727.1:p.Gly263= | |
| NM_172057.3:c.789C>T | NP_742054.1:p.Gly263= |