Canonical Allele Identifier: CA473651209
Gene:

Linked Data

MyVariant Identifiers: chr11:g.27505665A>C (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.27484118A>C , CM000673.2:g.27484118A>C GRCh38
NC_000011.9:g.27505665A>C , CM000673.1:g.27505665A>C GRCh37
NC_000011.8:g.27462241A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000496450.1:n.269A>C
Search 100 bp 5'
Search 100 bp 3'