Canonical Allele Identifier: CA520116165
Gene: BCORP1 HGNC NCBI

Linked Data

dbSNP Id: rs1603543715
MyVariant Identifiers: chrY:g.21644274T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19482388T>A , CM000686.2:g.19482388T>A GRCh38
NC_000024.9:g.21644274T>A , CM000686.1:g.21644274T>A GRCh37
NC_000024.8:g.20103662T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000650676.1:n.112-2094A>T
ENST00000400605.5:n.106-2094A>T
ENST00000441139.5:n.123-2094A>T
ENST00000513194.1:n.2497A>T
NR_002923.2:n.123-2094A>T
NR_033732.1:n.123-2094A>T