Canonical Allele Identifier: CA2766252020
Gene: BCORP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19466848T>C , CM000686.2:g.19466848T>C GRCh38
NC_000024.9:g.21628734T>C , CM000686.1:g.21628734T>C GRCh37
NC_000024.8:g.20088122T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000650676.1:n.1268A>G
ENST00000400605.5:n.1262A>G
ENST00000441139.5:n.1279A>G
ENST00000513194.1:n.4316-141A>G
NR_002923.2:n.1279A>G
NR_033732.1:n.1279A>G