Canonical Allele Identifier: CA2766251984
Gene: BCORP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19466412C>T , CM000686.2:g.19466412C>T GRCh38
NC_000024.9:g.21628298C>T , CM000686.1:g.21628298C>T GRCh37
NC_000024.8:g.20087686C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000650676.1:n.1660+44G>A
ENST00000400605.5:n.1654+44G>A
ENST00000441139.5:n.1671+44G>A
ENST00000513194.1:n.4579+32G>A
NR_002923.2:n.1671+44G>A
NR_033732.1:n.1671+44G>A