Canonical Allele Identifier: CA473651185
Gene:

Linked Data

MyVariant Identifiers: chr11:g.27505657G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.27484110G>C , CM000673.2:g.27484110G>C GRCh38
NC_000011.9:g.27505657G>C , CM000673.1:g.27505657G>C GRCh37
NC_000011.8:g.27462233G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000496450.1:n.261G>C