Canonical Allele Identifier: CA520118005
Gene: BCORP1 HGNC NCBI

Linked Data

dbSNP Id: rs2124148088
MyVariant Identifiers: chrY:g.21644868A>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19482982A>T , CM000686.2:g.19482982A>T GRCh38
NC_000024.9:g.21644868A>T , CM000686.1:g.21644868A>T GRCh37
NC_000024.8:g.20104256A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000650676.1:n.112-2688T>A
ENST00000400605.5:n.106-2688T>A
ENST00000441139.5:n.123-2688T>A
ENST00000513194.1:n.1903T>A
NR_002923.2:n.123-2688T>A
NR_033732.1:n.123-2688T>A
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