Canonical Allele Identifier: CA520128772
Gene: BCORP1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrY:g.21646518T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19484632T>A , CM000686.2:g.19484632T>A GRCh38
NC_000024.9:g.21646518T>A , CM000686.1:g.21646518T>A GRCh37
NC_000024.8:g.20105906T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000650676.1:n.112-4338A>T
ENST00000400605.5:n.106-4338A>T
ENST00000441139.5:n.123-4338A>T
ENST00000513194.1:n.253A>T
NR_002923.2:n.123-4338A>T
NR_033732.1:n.123-4338A>T