Canonical Allele Identifier: CA2844474211
Gene: BCORP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19466421G>A , CM000686.2:g.19466421G>A GRCh38
NC_000024.9:g.21628307G>A , CM000686.1:g.21628307G>A GRCh37
NC_000024.8:g.20087695G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000650676.1:n.1660+35C>T
ENST00000400605.5:n.1654+35C>T
ENST00000441139.5:n.1671+35C>T
ENST00000513194.1:n.4579+23C>T
NR_002923.2:n.1671+35C>T
NR_033732.1:n.1671+35C>T