Canonical Allele Identifier: CA2221132797
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.49108613C= , CM000678.2:g.49108613C= GRCh38
NC_000016.9:g.49142524C= , CM000678.1:g.49142524C= GRCh37
NC_000016.8:g.47700025C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_933517.1:n.810+1331G=
XR_001752138.2:n.591+5363G=
XR_933517.2:n.810+1331G=