Canonical Allele Identifier: CA520110646
Gene: BCORP1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrY:g.21628435T>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19466549T>A , CM000686.2:g.19466549T>A GRCh38
NC_000024.9:g.21628435T>A , CM000686.1:g.21628435T>A GRCh37
NC_000024.8:g.20087823T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000650676.1:n.1567A>T
ENST00000400605.5:n.1561A>T
ENST00000441139.5:n.1578A>T
ENST00000513194.1:n.4474A>T
NR_002923.2:n.1578A>T
NR_033732.1:n.1578A>T
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