Linked Data
dbSNP Id:
rs905114117
gnomAD v2:
5-11384863-C-T
gnomAD v4:
5-11384751-C-T
COSMIC:
COSM3784448
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.11384751C>T , CM000667.2:g.11384751C>T | GRCh38 |
| NC_000005.9:g.11384863C>T , CM000667.1:g.11384863C>T | GRCh37 |
| NC_000005.8:g.11437863C>T | NCBI36 |
| NG_023544.1:g.524248G>A | |
| NG_023544.2:g.524248G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000706271.1:c.167-19861G>A | ENSP00000516315.1:n.167-19861G>A | |
| ENST00000706272.1:c.163G>A | ||
| ENST00000304623.13:c.1091G>A MANE Select | ENSP00000307134.8:p.Arg364His | |
| ENST00000304623.12:c.1091G>A | ENSP00000307134.8:p.Arg364His | |
| ENST00000495388.6:n.21G>A | ||
| ENST00000502551.5:c.398-19861G>A | ENSP00000422389.1:n.398-19861G>A | |
| ENST00000503622.5:c.167-19861G>A | ENSP00000426887.1:n.167-19861G>A | |
| ENST00000504354.5:n.217-19861G>A | ||
| ENST00000504499.5:c.612+12280G>A | ENSP00000421000.1:n.612+12280G>A | |
| ENST00000506735.1:n.162G>A | ||
| ENST00000507430.1:n.187G>A | ||
| ENST00000511278.5:n.542-19861G>A | ||
| ENST00000511377.5:c.818G>A | ENSP00000426510.1:p.Arg273His | |
| ENST00000513588.5:c.440-19861G>A | ENSP00000421093.1:n.440-19861G>A | |
| NM_001288715.1:c.818G>A | NP_001275644.1:p.Arg273His | |
| NM_001288716.1:c.167-19861G>A | NP_001275645.1:n.167-19861G>A | |
| NM_001288717.1:c.-123+12280G>A | NP_001275646.1:n.-123+12280G>A | |
| NM_001332.3:c.1091G>A | NP_001323.1:p.Arg364His | |
| NR_109988.1:n.630-19861G>A | ||
| XM_005248251.2:c.1091G>A | XP_005248308.1:p.Arg364His | |
| XM_005248252.1:c.1049G>A | XP_005248309.1:p.Arg350His | |
| XM_005248253.1:c.818G>A | XP_005248310.1:p.Arg273His | |
| XM_011513967.1:c.818G>A | XP_011512269.1:p.Arg273His | |
| NM_001364128.1:c.167-19861G>A | NP_001351057.1:n.167-19861G>A | |
| XM_005248251.3:c.1091G>A | XP_005248308.1:p.Arg364His | |
| XM_005248252.2:c.1049G>A | XP_005248309.1:p.Arg350His | |
| XM_011513967.2:c.818G>A | XP_011512269.1:p.Arg273His | |
| XM_017009072.1:c.440-19861G>A | XP_016864561.1:n.440-19861G>A | |
| XM_017009073.1:c.398-19861G>A | XP_016864562.1:n.398-19861G>A | |
| XM_017009074.1:c.440-19861G>A | XP_016864563.1:n.440-19861G>A | |
| XM_017009075.2:c.167-19861G>A | XP_016864564.1:n.167-19861G>A | |
| XM_024454368.1:c.-325G>A | XP_024310136.1:n.-325G>A | |
| NM_001332.4:c.1091G>A MANE Select | NP_001323.1:p.Arg364His | |
| NM_001288717.2:c.-123+12280G>A | NP_001275646.1:n.-123+12280G>A | |
| NR_109988.2:n.1033-19861G>A | ||
| NM_001364128.2:c.167-19861G>A | NP_001351057.1:n.167-19861G>A |