Canonical Allele Identifier: CA2766251989
Gene: BCORP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19466437T>C , CM000686.2:g.19466437T>C GRCh38
NC_000024.9:g.21628323T>C , CM000686.1:g.21628323T>C GRCh37
NC_000024.8:g.20087711T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000650676.1:n.1660+19A>G
ENST00000400605.5:n.1654+19A>G
ENST00000441139.5:n.1671+19A>G
ENST00000513194.1:n.4579+7A>G
NR_002923.2:n.1671+19A>G
NR_033732.1:n.1671+19A>G