Canonical Allele Identifier: CA1267947429
Gene:

Linked Data

dbSNP Id: rs1268433020

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88016235C>G , CM000664.2:g.88016235C>G GRCh38
NC_000002.11:g.88315754C>G , CM000664.1:g.88315754C>G GRCh37
NC_000002.10:g.88096869C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940335.3:n.580C>G
XR_940336.3:n.580C>G