Canonical Allele Identifier: CA680801477

Gene:

Linked Data

• dbSNP Id: rs1271835037
• MyVariant Identifiers: chr11:g.80562772C>A (hg19) ; chr11:g.80851729C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.80851729C>A , CM000673.2:g.80851729C>A	GRCh38
NC_000011.9:g.80562772C>A , CM000673.1:g.80562772C>A	GRCh37
NC_000011.8:g.80240420C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_247272.2:n.124+60562G>T