Canonical Allele Identifier: CA427349373
Gene:

Linked Data

dbSNP Id: rs200827761
MyVariant Identifiers: chr2:g.88315884C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88016365C>G , CM000664.2:g.88016365C>G GRCh38
NC_000002.11:g.88315884C>G , CM000664.1:g.88315884C>G GRCh37
NC_000002.10:g.88096999C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940335.3:n.710C>G
XR_940336.3:n.710C>G