Canonical Allele Identifier: CA337396380
Gene: BCORP1 HGNC NCBI

Linked Data

dbSNP Id: rs72625366

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19482382T>G , CM000686.2:g.19482382T>G GRCh38
NC_000024.9:g.21644268T>G , CM000686.1:g.21644268T>G GRCh37
NC_000024.8:g.20103656T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000650676.1:n.112-2088A>C
ENST00000400605.5:n.106-2088A>C
ENST00000441139.5:n.123-2088A>C
ENST00000513194.1:n.2503A>C
NR_002923.2:n.123-2088A>C
NR_033732.1:n.123-2088A>C