Linked Data
ClinVar Variation Id:
645343
ClinVar RCV Id:
RCV000799403
dbSNP Id:
rs767398783
ExAC:
15:42693866 G / A
gnomAD v2:
15-42693866-G-A
gnomAD v3:
15-42401668-G-A
gnomAD v4:
15-42401668-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.42401668G>A , CM000677.2:g.42401668G>A | GRCh38 |
| NC_000015.9:g.42693866G>A , CM000677.1:g.42693866G>A | GRCh37 |
| NC_000015.8:g.40481158G>A | NCBI36 |
| NG_008660.1:g.58566G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000349748.8:c.1238G>A | ENSP00000183936.4:p.Arg413His | |
| ENST00000357568.8:c.1382G>A | ENSP00000350181.3:p.Arg461His | |
| ENST00000397163.8:c.1382G>A MANE Select | ENSP00000380349.3:p.Arg461His | |
| ENST00000466369.5:n.1891G>A | ||
| ENST00000483208.5:n.1613G>A | ||
| ENST00000495723.1:n.1613G>A | ||
| ENST00000549793.5:n.1613G>A | ||
| ENST00000638141.2:n.1253G>A | ||
| ENST00000673705.1:c.309+2016G>A | ENSP00000501021.1:n.309+2016G>A | |
| ENST00000318023.11:c.1238G>A | ENSP00000326281.8:p.Arg413His | |
| ENST00000349748.7:c.1238G>A | ENSP00000183936.4:p.Arg413His | |
| ENST00000357568.7:c.1382G>A | ENSP00000350181.3:p.Arg461His | |
| ENST00000397163.7:c.1382G>A | ENSP00000380349.3:p.Arg461His | |
| NM_000070.2:c.1382G>A | NP_000061.1:p.Arg461His | |
| NM_024344.1:c.1382G>A | NP_077320.1:p.Arg461His | |
| NM_173087.1:c.1238G>A | NP_775110.1:p.Arg413His | |
| NM_000070.3:c.1382G>A MANE Select | NP_000061.1:p.Arg461His | |
| NM_024344.2:c.1382G>A | NP_077320.1:p.Arg461His | |
| NM_173087.2:c.1238G>A | NP_775110.1:p.Arg413His |