Canonical Allele Identifier: CA923857074
Gene: BCORP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19466422C>T , CM000686.2:g.19466422C>T GRCh38
NC_000024.9:g.21628308C>T , CM000686.1:g.21628308C>T GRCh37
NC_000024.8:g.20087696C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000650676.1:n.1660+34G>A
ENST00000400605.5:n.1654+34G>A
ENST00000441139.5:n.1671+34G>A
ENST00000513194.1:n.4579+22G>A
NR_002923.2:n.1671+34G>A
NR_033732.1:n.1671+34G>A