Canonical Allele Identifier: CA427349429
Gene:

Linked Data

MyVariant Identifiers: chr2:g.88315906C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88016387C>A , CM000664.2:g.88016387C>A GRCh38
NC_000002.11:g.88315906C>A , CM000664.1:g.88315906C>A GRCh37
NC_000002.10:g.88097021C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940335.3:n.732C>A
XR_940336.3:n.732C>A
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