Canonical Allele Identifier: CA476175400

Gene:

Linked Data

• gnomAD v4: 11-89733478-T-A
• MyVariant Identifiers: chr11:g.89466646T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.89733478T>A , CM000673.2:g.89733478T>A	GRCh38
NC_000011.9:g.89466646T>A , CM000673.1:g.89466646T>A	GRCh37
NC_000011.8:g.89106294T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000527668.1:n.2462T>A