Canonical Allele Identifier: CA427349478
Gene:

Linked Data

MyVariant Identifiers: chr2:g.88315929A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88016410A>C , CM000664.2:g.88016410A>C GRCh38
NC_000002.11:g.88315929A>C , CM000664.1:g.88315929A>C GRCh37
NC_000002.10:g.88097044A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940335.3:n.755A>C
XR_940336.3:n.755A>C