Canonical Allele Identifier: CA772782702
Gene:

Linked Data

dbSNP Id: rs1294644111

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50211735G>A , CM000679.2:g.50211735G>A GRCh38
NC_000017.10:g.48289096G>A , CM000679.1:g.48289096G>A GRCh37
NC_000017.9:g.45644095G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_934838.1:n.43-2100G>A