Canonical Allele Identifier: CA173689896

Gene:

Linked Data

• dbSNP Id: rs866748975
• MyVariant Identifiers: chr8:g.20592453C>G (hg19) ; chr8:g.20734942C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.20734942C>G , CM000670.2:g.20734942C>G	GRCh38
NC_000008.10:g.20592453C>G , CM000670.1:g.20592453C>G	GRCh37
NC_000008.9:g.20636733C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_949569.3:n.72-55504C>G