Linked Data
ClinVar Variation Id:
284133
dbSNP Id:
rs372401631
ExAC:
15:42684911 G / T
gnomAD v2:
15-42684911-G-T
gnomAD v3:
15-42392713-G-T
gnomAD v4:
15-42392713-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.42392713G>T , CM000677.2:g.42392713G>T | GRCh38 |
| NC_000015.9:g.42684911G>T , CM000677.1:g.42684911G>T | GRCh37 |
| NC_000015.8:g.40472203G>T | NCBI36 |
| NG_008660.1:g.49611G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000349748.8:c.876G>T | ENSP00000183936.4:p.Gly292= | |
| ENST00000357568.8:c.1020G>T | ENSP00000350181.3:p.Gly340= | |
| ENST00000397163.8:c.1020G>T MANE Select | ENSP00000380349.3:p.Gly340= | |
| ENST00000466369.5:n.1529G>T | ||
| ENST00000483208.5:n.1251G>T | ||
| ENST00000495723.1:n.1251G>T | ||
| ENST00000549793.5:n.1251G>T | ||
| ENST00000638141.2:n.891G>T | ||
| ENST00000673658.1:n.4G>T | ||
| ENST00000673705.1:c.71-4087G>T | ENSP00000501021.1:n.71-4087G>T | |
| ENST00000318023.11:c.876G>T | ENSP00000326281.8:p.Gly292= | |
| ENST00000349748.7:c.876G>T | ENSP00000183936.4:p.Gly292= | |
| ENST00000357568.7:c.1020G>T | ENSP00000350181.3:p.Gly340= | |
| ENST00000397163.7:c.1020G>T | ENSP00000380349.3:p.Gly340= | |
| NM_000070.2:c.1020G>T | NP_000061.1:p.Gly340= | |
| NM_024344.1:c.1020G>T | NP_077320.1:p.Gly340= | |
| NM_173087.1:c.876G>T | NP_775110.1:p.Gly292= | |
| NM_000070.3:c.1020G>T MANE Select | NP_000061.1:p.Gly340= | |
| NM_024344.2:c.1020G>T | NP_077320.1:p.Gly340= | |
| NM_173087.2:c.876G>T | NP_775110.1:p.Gly292= |