Canonical Allele Identifier: CA849634258

Gene:

Linked Data

• dbSNP Id: rs1252557277
• MyVariant Identifiers: chr8:g.19987558A>G (hg19) ; chr8:g.20130047A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.20130047A>G , CM000670.2:g.20130047A>G	GRCh38
NC_000008.10:g.19987558A>G , CM000670.1:g.19987558A>G	GRCh37
NC_000008.9:g.20031838A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_949563.1:n.3408+128A>G
XR_949563.2:n.3400+128A>G