Canonical Allele Identifier: CA202788793
Gene:

Linked Data

dbSNP Id: rs996431827

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.8697633G>A , CM000672.2:g.8697633G>A GRCh38
NC_000010.10:g.8739596G>A , CM000672.1:g.8739596G>A GRCh37
NC_000010.9:g.8779602G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_930641.1:n.33-27832C>T