Canonical Allele Identifier: CA520117928
Gene: BCORP1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrY:g.21644843G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19482957G>C , CM000686.2:g.19482957G>C GRCh38
NC_000024.9:g.21644843G>C , CM000686.1:g.21644843G>C GRCh37
NC_000024.8:g.20104231G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000650676.1:n.112-2663C>G
ENST00000400605.5:n.106-2663C>G
ENST00000441139.5:n.123-2663C>G
ENST00000513194.1:n.1928C>G
NR_002923.2:n.123-2663C>G
NR_033732.1:n.123-2663C>G