Canonical Allele Identifier: CA219833907

Gene:

Linked Data

• dbSNP Id: rs182903596
• gnomAD v2: 11-27505671-G-A
• gnomAD v3: 11-27484124-G-A
• gnomAD v4: 11-27484124-G-A
• MyVariant Identifiers: chr11:g.27505671G>A (hg19) ; chr11:g.27484124G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.27484124G>A , CM000673.2:g.27484124G>A	GRCh38
NC_000011.9:g.27505671G>A , CM000673.1:g.27505671G>A	GRCh37
NC_000011.8:g.27462247G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496450.1:n.275G>A