Linked Data
ClinVar Variation Id:
1142031
ClinVar RCV Id:
RCV001479693
dbSNP Id:
rs2151217005
gnomAD v4:
15-73329678-G-T
MyVariant Identifiers:
chr15:g.73622019G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.73329678G>T , CM000677.2:g.73329678G>T | GRCh38 |
| NC_000015.9:g.73622019G>T , CM000677.1:g.73622019G>T | GRCh37 |
| NC_000015.8:g.71409072G>T | NCBI36 |
| NG_009063.1:g.44587C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261917.4:c.1485C>A MANE Select | ENSP00000261917.3:p.Thr495= | |
| ENST00000261917.3:c.1485C>A | ENSP00000261917.3:p.Thr495= | |
| NM_005477.2:c.1485C>A | NP_005468.1:p.Thr495= | |
| XM_011521148.1:c.267C>A | XP_011519450.1:p.Thr89= | |
| XM_011521148.2:c.267C>A | XP_011519450.1:p.Thr89= | |
| NM_005477.3:c.1485C>A MANE Select | NP_005468.1:p.Thr495= |