Canonical Allele Identifier: CA2221609001
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.50109073C= , CM000678.2:g.50109073C= GRCh38
NC_000016.9:g.50142984C= , CM000678.1:g.50142984C= GRCh37
NC_000016.8:g.48700485C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_011523490.1:c.115-2421G= XP_011521792.1:n.115-2421G=