Canonical Allele Identifier: CA473651210

Gene:

Linked Data

• gnomAD v4: 11-27484118-A-G
• MyVariant Identifiers: chr11:g.27505665A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.27484118A>G , CM000673.2:g.27484118A>G	GRCh38
NC_000011.9:g.27505665A>G , CM000673.1:g.27505665A>G	GRCh37
NC_000011.8:g.27462241A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496450.1:n.269A>G