Canonical Allele Identifier: CA680186685

Gene:

Linked Data

• dbSNP Id: rs1175088532
• MyVariant Identifiers: chr11:g.747028G>T (hg19) ; chr11:g.747028G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.747028G>T , CM000673.2:g.747028G>T	GRCh38
NC_000011.9:g.747028G>T , CM000673.1:g.747028G>T	GRCh37
NC_000011.8:g.737028G>T	NCBI36
NG_008160.1:g.4597G>T

Transcript Alleles

HGVS	Amino-acid change
XR_930963.1:n.259+179G>T