Canonical Allele Identifier: CA476175858
Gene:

Linked Data

MyVariant Identifiers: chr11:g.89466746T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.89733578T>A , CM000673.2:g.89733578T>A GRCh38
NC_000011.9:g.89466746T>A , CM000673.1:g.89466746T>A GRCh37
NC_000011.8:g.89106394T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000527668.1:n.2562T>A