Canonical Allele Identifier: CA427349431
Gene:

Linked Data

MyVariant Identifiers: chr2:g.88315906C>T (hg19)

Genomic Alleles

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

Transcript Alleles

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