Canonical Allele Identifier: CA427349390
Gene:

Linked Data

MyVariant Identifiers: chr2:g.88315891G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88016372G>C , CM000664.2:g.88016372G>C GRCh38
NC_000002.11:g.88315891G>C , CM000664.1:g.88315891G>C GRCh37
NC_000002.10:g.88097006G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940335.3:n.717G>C
XR_940336.3:n.717G>C