Canonical Allele Identifier: CA1267947303
Gene:

Linked Data

dbSNP Id: rs746043342

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88016123T>A , CM000664.2:g.88016123T>A GRCh38
NC_000002.11:g.88315642T>A , CM000664.1:g.88315642T>A GRCh37
NC_000002.10:g.88096757T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940335.3:n.468T>A
XR_940336.3:n.468T>A