Canonical Allele Identifier: CA520117393
Gene: BCORP1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrY:g.21644663A>C (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19482777A>C , CM000686.2:g.19482777A>C GRCh38
NC_000024.9:g.21644663A>C , CM000686.1:g.21644663A>C GRCh37
NC_000024.8:g.20104051A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000650676.1:n.112-2483T>G
ENST00000400605.5:n.106-2483T>G
ENST00000441139.5:n.123-2483T>G
ENST00000513194.1:n.2108T>G
NR_002923.2:n.123-2483T>G
NR_033732.1:n.123-2483T>G
Search 100 bp 5'
Search 100 bp 3'