Canonical Allele Identifier: CA772250089

Gene:

Linked Data

• dbSNP Id: rs1387110443
• gnomAD v4: 17-43952732-A-C
• MyVariant Identifiers: chr17:g.42030100A>C (hg19) ; chr17:g.43952732A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43952732A>C , CM000679.2:g.43952732A>C	GRCh38
NC_000017.10:g.42030100A>C , CM000679.1:g.42030100A>C	GRCh37
NC_000017.9:g.39385626A>C	NCBI36
NG_023338.1:g.56738T>G