Canonical Allele Identifier: CA2470906501
Gene: BCORP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19512141G= , CM000686.2:g.19512141G= GRCh38
NC_000024.9:g.21674027G= , CM000686.1:g.21674027G= GRCh37
NC_000024.8:g.20133415G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000650676.1:n.112-31847C=