Canonical Allele Identifier: CA1267947380
Gene:

Linked Data

dbSNP Id: rs1672676507

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88016197A>G , CM000664.2:g.88016197A>G GRCh38
NC_000002.11:g.88315716A>G , CM000664.1:g.88315716A>G GRCh37
NC_000002.10:g.88096831A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_940335.3:n.542A>G
XR_940336.3:n.542A>G