Canonical Allele Identifier: CA473651169

Gene:

Linked Data

• gnomAD v4: 11-27484105-C-A
• MyVariant Identifiers: chr11:g.27505652C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.27484105C>A , CM000673.2:g.27484105C>A	GRCh38
NC_000011.9:g.27505652C>A , CM000673.1:g.27505652C>A	GRCh37
NC_000011.8:g.27462228C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496450.1:n.256C>A