Canonical Allele Identifier: CA473651098
Gene:

Linked Data

MyVariant Identifiers: chr11:g.27505627T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.27484080T>C , CM000673.2:g.27484080T>C GRCh38
NC_000011.9:g.27505627T>C , CM000673.1:g.27505627T>C GRCh37
NC_000011.8:g.27462203T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000496450.1:n.231T>C