Canonical Allele Identifier: CA1267947390
Gene:

Linked Data

dbSNP Id: rs530118275

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88016205C>G , CM000664.2:g.88016205C>G GRCh38
NC_000002.11:g.88315724C>G , CM000664.1:g.88315724C>G GRCh37
NC_000002.10:g.88096839C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940335.3:n.550C>G
XR_940336.3:n.550C>G