Linked Data
ClinVar Variation Id:
1284887
ClinVar RCV Id:
RCV001699909
dbSNP Id:
rs2140288687
gnomAD v4:
15-71811519-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.71811519A>G , CM000677.2:g.71811519A>G | GRCh38 |
| NC_000015.9:g.72103859A>G , CM000677.1:g.72103859A>G | GRCh37 |
| NC_000015.8:g.69890913A>G | NCBI36 |
| NG_009113.2:g.5965A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000617575.5:c.155A>G MANE Select | ENSP00000482504.1:p.Asp52Gly | |
| ENST00000617575.4:c.155A>G | ENSP00000482504.1:p.Asp52Gly | |
| ENST00000621098.1:c.155A>G | ENSP00000479962.1:p.Asp52Gly | |
| ENST00000621736.4:c.-110A>G | ENSP00000479254.1:n.-110A>G | |
| NM_014249.3:c.155A>G | NP_055064.1:p.Asp52Gly | |
| NM_016346.3:c.155A>G | NP_057430.1:p.Asp52Gly | |
| XM_011521146.1:c.-110A>G | XP_011519448.1:n.-110A>G | |
| NM_014249.4:c.155A>G MANE Select | NP_055064.1:p.Asp52Gly | |
| NM_016346.4:c.155A>G | NP_057430.1:p.Asp52Gly |