Canonical Allele Identifier: CA427349364
Gene:

Linked Data

MyVariant Identifiers: chr2:g.88315881C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88016362C>T , CM000664.2:g.88016362C>T GRCh38
NC_000002.11:g.88315881C>T , CM000664.1:g.88315881C>T GRCh37
NC_000002.10:g.88096996C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940335.3:n.707C>T
XR_940336.3:n.707C>T