Canonical Allele Identifier: CA473651136

Gene:

Linked Data

• dbSNP Id: rs1364856623
• gnomAD v3: 11-27484093-G-T
• gnomAD v4: 11-27484093-G-T
• MyVariant Identifiers: chr11:g.27505640G>T (hg19) ; chr11:g.27484093G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.27484093G>T , CM000673.2:g.27484093G>T	GRCh38
NC_000011.9:g.27505640G>T , CM000673.1:g.27505640G>T	GRCh37
NC_000011.8:g.27462216G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496450.1:n.244G>T