Canonical Allele Identifier: CA520117125
Gene: BCORP1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrY:g.21644573C>G (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19482687C>G , CM000686.2:g.19482687C>G GRCh38
NC_000024.9:g.21644573C>G , CM000686.1:g.21644573C>G GRCh37
NC_000024.8:g.20103961C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000650676.1:n.112-2393G>C
ENST00000400605.5:n.106-2393G>C
ENST00000441139.5:n.123-2393G>C
ENST00000513194.1:n.2198G>C
NR_002923.2:n.123-2393G>C
NR_033732.1:n.123-2393G>C
Search 100 bp 5'
Search 100 bp 3'