Canonical Allele Identifier: CA473651095
Gene:

Linked Data

MyVariant Identifiers: chr11:g.27505626G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.27484079G>C , CM000673.2:g.27484079G>C GRCh38
NC_000011.9:g.27505626G>C , CM000673.1:g.27505626G>C GRCh37
NC_000011.8:g.27462202G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000496450.1:n.230G>C