Canonical Allele Identifier: CA2470903883
Gene: BCORP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19466237T= , CM000686.2:g.19466237T= GRCh38
NC_000024.9:g.21628123T= , CM000686.1:g.21628123T= GRCh37
NC_000024.8:g.20087511T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000650676.1:n.1660+219A=
ENST00000400605.5:n.1654+219A=
ENST00000441139.5:n.1671+219A=
ENST00000513194.1:n.4579+207A=
NR_002923.2:n.1671+219A=
NR_033732.1:n.1671+219A=