Canonical Allele Identifier: CA520115880
Gene: BCORP1 HGNC NCBI

Linked Data

gnomAD v3: Y-19482292-T-C
gnomAD v4: Y-19482292-T-C
MyVariant Identifiers: chrY:g.21644178T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19482292T>C , CM000686.2:g.19482292T>C GRCh38
NC_000024.9:g.21644178T>C , CM000686.1:g.21644178T>C GRCh37
NC_000024.8:g.20103566T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000650676.1:n.112-1998A>G
ENST00000400605.5:n.106-1998A>G
ENST00000441139.5:n.123-1998A>G
ENST00000513194.1:n.2593A>G
NR_002923.2:n.123-1998A>G
NR_033732.1:n.123-1998A>G