Canonical Allele Identifier: CA923738772
Gene: BCORP1 HGNC NCBI

Linked Data

dbSNP Id: rs2045081066
gnomAD v3: Y-19503646-C-T
gnomAD v4: Y-19503646-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19503646C>T , CM000686.2:g.19503646C>T GRCh38
NC_000024.9:g.21665532C>T , CM000686.1:g.21665532C>T GRCh37
NC_000024.8:g.20124920C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000650676.1:n.112-23352G>A