Canonical Allele Identifier: CA225746504

Gene:

Linked Data

• dbSNP Id: rs527730818
• MyVariant Identifiers: chr11:g.80854472T>C (hg19) ; chr11:g.81143429T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.81143429T>C , CM000673.2:g.81143429T>C	GRCh38
NC_000011.9:g.80854472T>C , CM000673.1:g.80854472T>C	GRCh37
NC_000011.8:g.80532120T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_247272.2:n.46+109497A>G