Canonical Allele Identifier: CA2573144668
Gene:

Linked Data

ClinVar Variation Id: 1353709
ClinVar RCV Id: RCV001873928
dbSNP Id: rs2131811086
gnomAD v4: 9-35658105-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.35658105T>A , CM000671.2:g.35658105T>A GRCh38
NC_000009.11:g.35658102T>A , CM000671.1:g.35658102T>A GRCh37
NC_000009.10:g.35648102T>A NCBI36
NG_017041.1:g.4914A>T , LRG_163:g.4914A>T
NG_033120.1:g.4816T>A