Canonical Allele Identifier: CA2470904993
Gene: BCORP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19482143T= , CM000686.2:g.19482143T= GRCh38
NC_000024.9:g.21644029T= , CM000686.1:g.21644029T= GRCh37
NC_000024.8:g.20103417T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000650676.1:n.112-1849A=
ENST00000400605.5:n.106-1849A=
ENST00000441139.5:n.123-1849A=
ENST00000513194.1:n.2742A=
NR_002923.2:n.123-1849A=
NR_033732.1:n.123-1849A=