Canonical Allele Identifier: CA2766251964
Gene: BCORP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19466346G>A , CM000686.2:g.19466346G>A GRCh38
NC_000024.9:g.21628232G>A , CM000686.1:g.21628232G>A GRCh37
NC_000024.8:g.20087620G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000650676.1:n.1660+110C>T
ENST00000400605.5:n.1654+110C>T
ENST00000441139.5:n.1671+110C>T
ENST00000513194.1:n.4579+98C>T
NR_002923.2:n.1671+110C>T
NR_033732.1:n.1671+110C>T