Canonical Allele Identifier: CA2766252284
Gene: BCORP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19484886T>C , CM000686.2:g.19484886T>C GRCh38
NC_000024.9:g.21646772T>C , CM000686.1:g.21646772T>C GRCh37
NC_000024.8:g.20106160T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000650676.1:n.112-4592A>G
ENST00000400605.5:n.106-4592A>G
ENST00000441139.5:n.123-4592A>G
NR_002923.2:n.123-4592A>G
NR_033732.1:n.123-4592A>G