Canonical Allele Identifier: CA473651159

Gene:

Linked Data

• dbSNP Id: rs1330150684
• gnomAD v3: 11-27484101-A-G
• gnomAD v4: 11-27484101-A-G
• MyVariant Identifiers: chr11:g.27505648A>G (hg19) ; chr11:g.27484101A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.27484101A>G , CM000673.2:g.27484101A>G	GRCh38
NC_000011.9:g.27505648A>G , CM000673.1:g.27505648A>G	GRCh37
NC_000011.8:g.27462224A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496450.1:n.252A>G