Canonical Allele Identifier: CA473651223

Gene:

Linked Data

• MyVariant Identifiers: chr11:g.27505670C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.27484123C>G , CM000673.2:g.27484123C>G	GRCh38
NC_000011.9:g.27505670C>G , CM000673.1:g.27505670C>G	GRCh37
NC_000011.8:g.27462246C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496450.1:n.274C>G