Canonical Allele Identifier: CA894254380
Gene:

Linked Data

dbSNP Id: rs1467504285

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88016237C>G , CM000664.2:g.88016237C>G GRCh38
NC_000002.11:g.88315756C>G , CM000664.1:g.88315756C>G GRCh37
NC_000002.10:g.88096871C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940335.3:n.582C>G
XR_940336.3:n.582C>G