Canonical Allele Identifier: CA520117109
Gene: BCORP1 HGNC NCBI

Linked Data

dbSNP Id: rs1603543724
MyVariant Identifiers: chrY:g.21644568G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19482682G>A , CM000686.2:g.19482682G>A GRCh38
NC_000024.9:g.21644568G>A , CM000686.1:g.21644568G>A GRCh37
NC_000024.8:g.20103956G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000650676.1:n.112-2388C>T
ENST00000400605.5:n.106-2388C>T
ENST00000441139.5:n.123-2388C>T
ENST00000513194.1:n.2203C>T
NR_002923.2:n.123-2388C>T
NR_033732.1:n.123-2388C>T
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