Canonical Allele Identifier: CA2523149742
Gene: BCORP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19475973T>C , CM000686.2:g.19475973T>C GRCh38
NC_000024.9:g.21637859T>C , CM000686.1:g.21637859T>C GRCh37
NC_000024.8:g.20097247T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000650676.1:n.238-1070A>G
ENST00000400605.5:n.232-1070A>G
ENST00000441139.5:n.249-1070A>G
ENST00000513194.1:n.3397-1075A>G
NR_002923.2:n.249-1070A>G
NR_033732.1:n.249-1070A>G