Canonical Allele Identifier: CA2589318795
Gene: BCORP1 HGNC NCBI

Linked Data

dbSNP Id: rs2124147174

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19475862del , CM000686.2:g.19475862del GRCh38
NC_000024.9:g.21637748del , CM000686.1:g.21637748del GRCh37
NC_000024.8:g.20097136del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000650676.1:n.238-959del
ENST00000400605.5:n.232-959del
ENST00000441139.5:n.249-959del
ENST00000513194.1:n.3397-964del
NR_002923.2:n.249-959del
NR_033732.1:n.249-959del