Canonical Allele Identifier: CA2573144667
Gene:

Linked Data

ClinVar Variation Id: 1370455
ClinVar RCV Id: RCV001871001
dbSNP Id: rs1421770576
gnomAD v4: 9-35658097-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.35658097C>A , CM000671.2:g.35658097C>A GRCh38
NC_000009.11:g.35658094C>A , CM000671.1:g.35658094C>A GRCh37
NC_000009.10:g.35648094C>A NCBI36
NG_017041.1:g.4922G>T , LRG_163:g.4922G>T
NG_033120.1:g.4808C>A