Canonical Allele Identifier: CA473651172
Gene:

Linked Data

MyVariant Identifiers: chr11:g.27505653T>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.27484106T>A , CM000673.2:g.27484106T>A GRCh38
NC_000011.9:g.27505653T>A , CM000673.1:g.27505653T>A GRCh37
NC_000011.8:g.27462229T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000496450.1:n.257T>A
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