Canonical Allele Identifier: CA2510244342
Gene: BCORP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19512534T>C , CM000686.2:g.19512534T>C GRCh38
NC_000024.9:g.21674420T>C , CM000686.1:g.21674420T>C GRCh37
NC_000024.8:g.20133808T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000650676.1:n.112-32240A>G