Canonical Allele Identifier: CA1267947264
Gene:

Linked Data

dbSNP Id: rs1046001582

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88016075C>G , CM000664.2:g.88016075C>G GRCh38
NC_000002.11:g.88315594C>G , CM000664.1:g.88315594C>G GRCh37
NC_000002.10:g.88096709C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940335.3:n.420C>G
XR_940336.3:n.420C>G