Canonical Allele Identifier: CA520118040
Gene: BCORP1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrY:g.21644880T>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19482994T>G , CM000686.2:g.19482994T>G GRCh38
NC_000024.9:g.21644880T>G , CM000686.1:g.21644880T>G GRCh37
NC_000024.8:g.20104268T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000650676.1:n.112-2700A>C
ENST00000400605.5:n.106-2700A>C
ENST00000441139.5:n.123-2700A>C
ENST00000513194.1:n.1891A>C
NR_002923.2:n.123-2700A>C
NR_033732.1:n.123-2700A>C
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