Canonical Allele Identifier: CA173376449

Gene:

Linked Data

• dbSNP Id: rs1000162163
• MyVariant Identifiers: chr8:g.19987548A>G (hg19) ; chr8:g.20130037A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.20130037A>G , CM000670.2:g.20130037A>G	GRCh38
NC_000008.10:g.19987548A>G , CM000670.1:g.19987548A>G	GRCh37
NC_000008.9:g.20031828A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_949563.1:n.3408+118A>G
XR_949563.2:n.3400+118A>G