Canonical Allele Identifier: CA923857084
Gene: BCORP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19466443C>A , CM000686.2:g.19466443C>A GRCh38
NC_000024.9:g.21628329C>A , CM000686.1:g.21628329C>A GRCh37
NC_000024.8:g.20087717C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000650676.1:n.1660+13G>T
ENST00000400605.5:n.1654+13G>T
ENST00000441139.5:n.1671+13G>T
ENST00000513194.1:n.4579+1G>T
NR_002923.2:n.1671+13G>T
NR_033732.1:n.1671+13G>T