Canonical Allele Identifier: CA202788794
Gene:

Linked Data

dbSNP Id: rs940337737
gnomAD v3: 10-8697637-T-A
gnomAD v4: 10-8697637-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.8697637T>A , CM000672.2:g.8697637T>A GRCh38
NC_000010.10:g.8739600T>A , CM000672.1:g.8739600T>A GRCh37
NC_000010.9:g.8779606T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_930641.1:n.33-27836A>T