Canonical Allele Identifier: CA473651211
Gene:

Linked Data

MyVariant Identifiers: chr11:g.27505666A>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.27484119A>C , CM000673.2:g.27484119A>C GRCh38
NC_000011.9:g.27505666A>C , CM000673.1:g.27505666A>C GRCh37
NC_000011.8:g.27462242A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000496450.1:n.270A>C
Search 100 bp 5'
Search 100 bp 3'