Canonical Allele Identifier: CA473651195

Gene:

Linked Data

• gnomAD v4: 11-27484113-A-T
• MyVariant Identifiers: chr11:g.27505660A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.27484113A>T , CM000673.2:g.27484113A>T	GRCh38
NC_000011.9:g.27505660A>T , CM000673.1:g.27505660A>T	GRCh37
NC_000011.8:g.27462236A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000496450.1:n.264A>T