Canonical Allele Identifier: CA520117166
Gene: BCORP1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrY:g.21644587T>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19482701T>A , CM000686.2:g.19482701T>A GRCh38
NC_000024.9:g.21644587T>A , CM000686.1:g.21644587T>A GRCh37
NC_000024.8:g.20103975T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000650676.1:n.112-2407A>T
ENST00000400605.5:n.106-2407A>T
ENST00000441139.5:n.123-2407A>T
ENST00000513194.1:n.2184A>T
NR_002923.2:n.123-2407A>T
NR_033732.1:n.123-2407A>T
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