Linked Data
ClinVar Variation Id:
386963
ClinVar RCV Id:
RCV000426773
dbSNP Id:
rs548333586
ExAC:
17:62018365 G / A
gnomAD v2:
17-62018365-G-A
gnomAD v4:
17-63941005-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.63941005G>A , CM000679.2:g.63941005G>A | GRCh38 |
| NC_000017.10:g.62018365G>A , CM000679.1:g.62018365G>A | GRCh37 |
| NC_000017.9:g.59372097G>A | NCBI36 |
| NG_011699.1:g.36914C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000435607.3:c.5277C>T MANE Select | ENSP00000396320.1:p.Asp1759= | |
| ENST00000578147.5:c.5277C>T | ENSP00000463963.1:p.Asp1759= | |
| NM_000334.4:c.5277C>T MANE Select | NP_000325.4:p.Asp1759= | |
| XM_005257566.3:c.5277C>T | XP_005257623.1:p.Asp1759= |