Canonical Allele Identifier: CA2766251969
Gene: BCORP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19466359C>T , CM000686.2:g.19466359C>T GRCh38
NC_000024.9:g.21628245C>T , CM000686.1:g.21628245C>T GRCh37
NC_000024.8:g.20087633C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000650676.1:n.1660+97G>A
ENST00000400605.5:n.1654+97G>A
ENST00000441139.5:n.1671+97G>A
ENST00000513194.1:n.4579+85G>A
NR_002923.2:n.1671+97G>A
NR_033732.1:n.1671+97G>A