Canonical Allele Identifier: CA16229545
Gene:

Linked Data

ClinVar Variation Id: 1252728
ClinVar RCV Id: RCV001661025
dbSNP Id: rs10042486
gnomAD v2: 5-63261329-C-T
gnomAD v3: 5-63965502-C-T
gnomAD v4: 5-63965502-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.63965502C>T , CM000667.2:g.63965502C>T GRCh38
NC_000005.9:g.63261329C>T , CM000667.1:g.63261329C>T GRCh37
NC_000005.8:g.63297085C>T NCBI36
NG_032816.1:g.1791G>A