Canonical Allele Identifier: CA520118539
Gene: BCORP1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrY:g.21645048C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19483162C>A , CM000686.2:g.19483162C>A GRCh38
NC_000024.9:g.21645048C>A , CM000686.1:g.21645048C>A GRCh37
NC_000024.8:g.20104436C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000650676.1:n.112-2868G>T
ENST00000400605.5:n.106-2868G>T
ENST00000441139.5:n.123-2868G>T
ENST00000513194.1:n.1723G>T
NR_002923.2:n.123-2868G>T
NR_033732.1:n.123-2868G>T