Canonical Allele Identifier: CA337395812
Gene: BCORP1 HGNC NCBI

Linked Data

dbSNP Id: rs35316681

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19466858dup , CM000686.2:g.19466858dup GRCh38
NC_000024.9:g.21628744dup , CM000686.1:g.21628744dup GRCh37
NC_000024.8:g.20088132dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000650676.1:n.1261dup
ENST00000400605.5:n.1255dup
ENST00000441139.5:n.1272dup
ENST00000513194.1:n.4316-148dup
NR_002923.2:n.1272dup
NR_033732.1:n.1272dup