Canonical Allele Identifier: CA520118568
Gene: BCORP1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrY:g.21645058T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19483172T>A , CM000686.2:g.19483172T>A GRCh38
NC_000024.9:g.21645058T>A , CM000686.1:g.21645058T>A GRCh37
NC_000024.8:g.20104446T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000650676.1:n.112-2878A>T
ENST00000400605.5:n.106-2878A>T
ENST00000441139.5:n.123-2878A>T
ENST00000513194.1:n.1713A>T
NR_002923.2:n.123-2878A>T
NR_033732.1:n.123-2878A>T