Canonical Allele Identifier: CA2470906518
Gene: BCORP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19512492T= , CM000686.2:g.19512492T= GRCh38
NC_000024.9:g.21674378T= , CM000686.1:g.21674378T= GRCh37
NC_000024.8:g.20133766T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000650676.1:n.112-32198A=