Canonical Allele Identifier: CA2470903898
Gene: BCORP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19466559T= , CM000686.2:g.19466559T= GRCh38
NC_000024.9:g.21628445T= , CM000686.1:g.21628445T= GRCh37
NC_000024.8:g.20087833T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000650676.1:n.1557A=
ENST00000400605.5:n.1551A=
ENST00000441139.5:n.1568A=
ENST00000513194.1:n.4464A=
NR_002923.2:n.1568A=
NR_033732.1:n.1568A=