Canonical Allele Identifier: CA2263926887
Gene:

Linked Data

dbSNP Id: rs1908567180

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50211636G>A , CM000679.2:g.50211636G>A GRCh38
NC_000017.10:g.48288997G>A , CM000679.1:g.48288997G>A GRCh37
NC_000017.9:g.45643996G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_934838.1:n.43-2199G>A