Canonical Allele Identifier: CA173689912

Gene:

Linked Data

• dbSNP Id: rs893935853
• MyVariant Identifiers: chr8:g.20592548C>A (hg19) ; chr8:g.20735037C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.20735037C>A , CM000670.2:g.20735037C>A	GRCh38
NC_000008.10:g.20592548C>A , CM000670.1:g.20592548C>A	GRCh37
NC_000008.9:g.20636828C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_949569.3:n.72-55409C>A