Canonical Allele Identifier: CA473651132

Gene:

Linked Data

• gnomAD v4: 11-27484092-C-A
• MyVariant Identifiers: chr11:g.27505639C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.27484092C>A , CM000673.2:g.27484092C>A	GRCh38
NC_000011.9:g.27505639C>A , CM000673.1:g.27505639C>A	GRCh37
NC_000011.8:g.27462215C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496450.1:n.243C>A