Canonical Allele Identifier: CA2500004677
Gene: BCORP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19475987C>A , CM000686.2:g.19475987C>A GRCh38
NC_000024.9:g.21637873C>A , CM000686.1:g.21637873C>A GRCh37
NC_000024.8:g.20097261C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000650676.1:n.238-1084G>T
ENST00000400605.5:n.232-1084G>T
ENST00000441139.5:n.249-1084G>T
ENST00000513194.1:n.3397-1089G>T
NR_002923.2:n.249-1084G>T
NR_033732.1:n.249-1084G>T