Linked Data
ClinVar Variation Id:
596306
dbSNP Id:
rs773827877
ExAC:
15:42691829 G / C
gnomAD v2:
15-42691829-G-C
gnomAD v4:
15-42399631-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.42399631G>C , CM000677.2:g.42399631G>C | GRCh38 |
| NC_000015.9:g.42691829G>C , CM000677.1:g.42691829G>C | GRCh37 |
| NC_000015.8:g.40479121G>C | NCBI36 |
| NG_008660.1:g.56529G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000349748.8:c.1189G>C | ENSP00000183936.4:p.Gly397Arg | |
| ENST00000357568.8:c.1333G>C | ENSP00000350181.3:p.Gly445Arg | |
| ENST00000397163.8:c.1333G>C MANE Select | ENSP00000380349.3:p.Gly445Arg | |
| ENST00000466369.5:n.1842G>C | ||
| ENST00000483208.5:n.1564G>C | ||
| ENST00000495723.1:n.1564G>C | ||
| ENST00000549793.5:n.1564G>C | ||
| ENST00000638141.2:n.1204G>C | ||
| ENST00000673658.1:n.317G>C | ||
| ENST00000673705.1:c.288G>C | ENSP00000501021.1:n.288G>C | |
| ENST00000318023.11:c.1189G>C | ENSP00000326281.8:p.Gly397Arg | |
| ENST00000349748.7:c.1189G>C | ENSP00000183936.4:p.Gly397Arg | |
| ENST00000357568.7:c.1333G>C | ENSP00000350181.3:p.Gly445Arg | |
| ENST00000397163.7:c.1333G>C | ENSP00000380349.3:p.Gly445Arg | |
| NM_000070.2:c.1333G>C | NP_000061.1:p.Gly445Arg | |
| NM_024344.1:c.1333G>C | NP_077320.1:p.Gly445Arg | |
| NM_173087.1:c.1189G>C | NP_775110.1:p.Gly397Arg | |
| NM_000070.3:c.1333G>C MANE Select | NP_000061.1:p.Gly445Arg | |
| NM_024344.2:c.1333G>C | NP_077320.1:p.Gly445Arg | |
| NM_173087.2:c.1189G>C | NP_775110.1:p.Gly397Arg |