Canonical Allele Identifier: CA473651162
Gene:

Linked Data

MyVariant Identifiers: chr11:g.27505649A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.27484102A>G , CM000673.2:g.27484102A>G GRCh38
NC_000011.9:g.27505649A>G , CM000673.1:g.27505649A>G GRCh37
NC_000011.8:g.27462225A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000496450.1:n.253A>G