Canonical Allele Identifier: CA173689910

Gene:

Linked Data

• dbSNP Id: rs1000041886
• MyVariant Identifiers: chr8:g.20592539C>G (hg19) ; chr8:g.20735028C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.20735028C>G , CM000670.2:g.20735028C>G	GRCh38
NC_000008.10:g.20592539C>G , CM000670.1:g.20592539C>G	GRCh37
NC_000008.9:g.20636819C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_949569.3:n.72-55418C>G