Canonical Allele Identifier: CA923741827
Gene: BCORP1 HGNC NCBI

Linked Data

gnomAD v3: Y-19512402-G-T
gnomAD v4: Y-19512402-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19512402G>T , CM000686.2:g.19512402G>T GRCh38
NC_000024.9:g.21674288G>T , CM000686.1:g.21674288G>T GRCh37
NC_000024.8:g.20133676G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000650676.1:n.112-32108C>A