Canonical Allele Identifier: CA2470905971
Gene: BCORP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19503553A= , CM000686.2:g.19503553A= GRCh38
NC_000024.9:g.21665439A= , CM000686.1:g.21665439A= GRCh37
NC_000024.8:g.20124827A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000650676.1:n.112-23259T=