Linked Data
ClinVar Variation Id:
720259
dbSNP Id:
rs56737889
ExAC:
1:155631119 G / A
gnomAD v2:
1-155631119-G-A
gnomAD v3:
1-155661328-G-A
gnomAD v4:
1-155661328-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.155661328G>A , CM000663.2:g.155661328G>A | GRCh38 |
| NC_000001.10:g.155631119G>A , CM000663.1:g.155631119G>A | GRCh37 |
| NC_000001.9:g.153897743G>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000355499.9:c.975C>T MANE Select | ENSP00000347686.4:p.His325= | |
| ENST00000295566.8:c.1113C>T | ENSP00000295566.4:p.His371= | |
| ENST00000311573.9:c.882C>T | ENSP00000311138.5:p.His294= | |
| ENST00000347088.9:c.975C>T | ENSP00000316079.6:p.His325= | |
| ENST00000354691.9:c.*239C>T | ENSP00000346722.5:n.*239C>T | |
| ENST00000355499.8:c.975C>T | ENSP00000347686.4:p.His325= | |
| ENST00000359205.9:c.942C>T | ENSP00000352134.5:p.His314= | |
| ENST00000361140.8:c.*473C>T | ENSP00000354716.4:n.*473C>T | |
| ENST00000361831.9:c.942C>T | ENSP00000355298.5:p.His314= | |
| ENST00000368330.6:c.975C>T | ENSP00000357314.2:p.His325= | |
| ENST00000368339.9:c.1389C>T | ENSP00000357323.5:p.His463= | |
| ENST00000368340.9:c.1329C>T | ENSP00000357324.5:p.His443= | |
| ENST00000404643.5:c.915C>T | ENSP00000385390.1:p.His305= | |
| ENST00000405763.7:c.1389C>T | ENSP00000384583.3:p.His463= | |
| ENST00000407221.5:c.882C>T | ENSP00000385791.1:p.His294= | |
| ENST00000436865.5:c.*984C>T | ENSP00000390116.1:n.*984C>T | |
| ENST00000442834.6:n.1019C>T | ||
| ENST00000477470.1:n.585C>T | ||
| ENST00000488784.5:n.668C>T | ||
| ENST00000493625.5:n.854C>T | ||
| NM_001198899.1:c.942C>T | NP_001185828.1:p.His314= | |
| NM_001198900.1:c.942C>T | NP_001185829.1:p.His314= | |
| NM_001198901.1:c.975C>T | NP_001185830.1:p.His325= | |
| NM_001198902.1:c.975C>T | NP_001185831.1:p.His325= | |
| NM_001198903.1:c.1389C>T | NP_001185832.1:p.His463= | |
| NM_001198904.1:c.1329C>T | NP_001185833.1:p.His443= | |
| NM_001198905.1:c.915C>T | NP_001185834.1:p.His305= | |
| NM_001198906.1:c.1173C>T | NP_001185835.1:p.His391= | |
| NM_018253.3:c.942C>T | NP_060723.2:p.His314= | |
| NM_139118.2:c.1113C>T | NP_620829.1:p.His371= | |
| NM_139119.2:c.975C>T | NP_620830.1:p.His325= | |
| NM_139121.2:c.777C>T | NP_620832.1:p.His259= | |
| XM_011509721.1:c.1173C>T | XP_011508023.1:p.His391= | |
| XM_011509722.1:c.942C>T | XP_011508024.1:p.His314= | |
| NM_001198906.2:c.1173C>T | NP_001185835.1:p.His391= | |
| NM_001198899.2:c.942C>T | NP_001185828.1:p.His314= | |
| NM_001198900.2:c.942C>T | NP_001185829.1:p.His314= | |
| NM_001198901.2:c.975C>T | NP_001185830.1:p.His325= | |
| NM_001198902.2:c.975C>T | NP_001185831.1:p.His325= | |
| NM_001198905.2:c.915C>T | NP_001185834.1:p.His305= | |
| NM_018253.4:c.942C>T | NP_060723.2:p.His314= | |
| NM_139118.3:c.1113C>T | NP_620829.1:p.His371= | |
| NM_139119.3:c.975C>T MANE Select | NP_620830.1:p.His325= | |
| NM_139121.3:c.777C>T | NP_620832.1:p.His259= |