Canonical Allele Identifier: CA225652657

Gene:

Linked Data

• dbSNP Id: rs1022076894
• MyVariant Identifiers: chr11:g.80562756C>T (hg19) ; chr11:g.80851713C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.80851713C>T , CM000673.2:g.80851713C>T	GRCh38
NC_000011.9:g.80562756C>T , CM000673.1:g.80562756C>T	GRCh37
NC_000011.8:g.80240404C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_247272.2:n.124+60578G>A