Canonical Allele Identifier: CA2766251961
Gene: BCORP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19466316G>T , CM000686.2:g.19466316G>T GRCh38
NC_000024.9:g.21628202G>T , CM000686.1:g.21628202G>T GRCh37
NC_000024.8:g.20087590G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000650676.1:n.1660+140C>A
ENST00000400605.5:n.1654+140C>A
ENST00000441139.5:n.1671+140C>A
ENST00000513194.1:n.4579+128C>A
NR_002923.2:n.1671+140C>A
NR_033732.1:n.1671+140C>A