Canonical Allele Identifier: CA427349342
Gene:

Linked Data

dbSNP Id: rs1172833437

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88016354A>G , CM000664.2:g.88016354A>G GRCh38
NC_000002.11:g.88315873A>G , CM000664.1:g.88315873A>G GRCh37
NC_000002.10:g.88096988A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940335.3:n.699A>G
XR_940336.3:n.699A>G