Canonical Allele Identifier: CA2470903888
Gene: BCORP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19466365A= , CM000686.2:g.19466365A= GRCh38
NC_000024.9:g.21628251A= , CM000686.1:g.21628251A= GRCh37
NC_000024.8:g.20087639A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000650676.1:n.1660+91T=
ENST00000400605.5:n.1654+91T=
ENST00000441139.5:n.1671+91T=
ENST00000513194.1:n.4579+79T=
NR_002923.2:n.1671+91T=
NR_033732.1:n.1671+91T=