Canonical Allele Identifier: CA2470908811
Gene: BCORP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19560382T= , CM000686.2:g.19560382T= GRCh38
NC_000024.9:g.21722268T= , CM000686.1:g.21722268T= GRCh37
NC_000024.8:g.20181656T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000650676.1:n.111+6600A=
ENST00000651484.1:n.71-2242A=
ENST00000693243.1:n.27-2242A=
XR_001756064.2:n.199-2242A=
XR_001756065.1:n.199-2242A=
XR_001756066.1:n.199-963A=
XR_938626.1:n.3173A=
XR_938626.2:n.3569A=
XR_938627.1:n.3173A=
XR_938627.2:n.3569A=
XR_938628.1:n.271-2242A=
XR_938628.3:n.199-2242A=
XR_938629.1:n.3173A=