Canonical Allele Identifier: CA1932346022
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.101750537C= , CM000672.2:g.101750537C= GRCh38
NC_000010.10:g.103510294C= , CM000672.1:g.103510294C= GRCh37
NC_000010.9:g.103500284C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_946255.1:n.217-6320G=
XR_946255.2:n.217-6320G=