Canonical Allele Identifier: CA2500480077
Gene: BCORP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19512437G>T , CM000686.2:g.19512437G>T GRCh38
NC_000024.9:g.21674323G>T , CM000686.1:g.21674323G>T GRCh37
NC_000024.8:g.20133711G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000650676.1:n.112-32143C>A