Canonical Allele Identifier: CA2569074538
Gene: BCORP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19512094C>T , CM000686.2:g.19512094C>T GRCh38
NC_000024.9:g.21673980C>T , CM000686.1:g.21673980C>T GRCh37
NC_000024.8:g.20133368C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000650676.1:n.112-31800G>A