Canonical Allele Identifier: CA427349351
Gene:

Linked Data

MyVariant Identifiers: chr2:g.88315876A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88016357A>T , CM000664.2:g.88016357A>T GRCh38
NC_000002.11:g.88315876A>T , CM000664.1:g.88315876A>T GRCh37
NC_000002.10:g.88096991A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940335.3:n.702A>T
XR_940336.3:n.702A>T