Canonical Allele Identifier: CA937524938
Gene:

Linked Data

dbSNP Id: rs1856778902

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.45506637C>A , CM000673.2:g.45506637C>A GRCh38
NC_000011.9:g.45528187C>A , CM000673.1:g.45528187C>A GRCh37
NC_000011.8:g.45484763C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001748204.2:n.909-16866G>T
XR_931245.3:n.566-16866G>T