Canonical Allele Identifier: CA2470905122
Gene: BCORP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19484857T= , CM000686.2:g.19484857T= GRCh38
NC_000024.9:g.21646743T= , CM000686.1:g.21646743T= GRCh37
NC_000024.8:g.20106131T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000650676.1:n.112-4563A=
ENST00000400605.5:n.106-4563A=
ENST00000441139.5:n.123-4563A=
ENST00000513194.1:n.28A=
NR_002923.2:n.123-4563A=
NR_033732.1:n.123-4563A=