Canonical Allele Identifier: CA427349424
Gene:

Linked Data

MyVariant Identifiers: chr2:g.88315904T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88016385T>A , CM000664.2:g.88016385T>A GRCh38
NC_000002.11:g.88315904T>A , CM000664.1:g.88315904T>A GRCh37
NC_000002.10:g.88097019T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940335.3:n.730T>A
XR_940336.3:n.730T>A