Linked Data
ClinVar Variation Id:
392468
dbSNP Id:
rs759083770
ExAC:
X:18646567 G / A
gnomAD v2:
X-18646567-G-A
gnomAD v3:
X-18628447-G-A
gnomAD v4:
X-18628447-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.18628447G>A , CM000685.2:g.18628447G>A | GRCh38 |
| NC_000023.10:g.18646567G>A , CM000685.1:g.18646567G>A | GRCh37 |
| NC_000023.9:g.18556488G>A | NCBI36 |
| NG_008475.1:g.207843G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000623535.2:c.2573G>A MANE Select | ENSP00000485244.1:p.Arg858His | |
| ENST00000674046.1:c.2696G>A | ENSP00000501174.1:p.Arg899His | |
| ENST00000379989.6:c.2573G>A | ENSP00000369325.3:p.Arg858His | |
| ENST00000379996.7:c.2573G>A | ENSP00000369332.3:p.Arg858His | |
| ENST00000623535.1:c.2573G>A | ENSP00000485244.1:p.Arg858His | |
| NM_001037343.1:c.2573G>A | NP_001032420.1:p.Arg858His | |
| NM_003159.2:c.2573G>A | NP_003150.1:p.Arg858His | |
| XM_011545569.1:c.2645G>A | XP_011543871.1:p.Arg882His | |
| XM_011545570.1:c.2564G>A | XP_011543872.1:p.Arg855His | |
| XR_950484.1:n.2948G>A | ||
| NM_001323289.1:c.2573G>A | NP_001310218.1:p.Arg858His | |
| NM_001323289.2:c.2573G>A MANE Select | NP_001310218.1:p.Arg858His | |
| NM_001037343.2:c.2573G>A | NP_001032420.1:p.Arg858His | |
| NM_003159.3:c.2573G>A | NP_003150.1:p.Arg858His |