Canonical Allele Identifier: CA923861373
Gene: BCORP1 HGNC NCBI

Linked Data

dbSNP Id: rs2045058704
gnomAD v3: Y-19475850-A-G
gnomAD v4: Y-19475850-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19475850A>G , CM000686.2:g.19475850A>G GRCh38
NC_000024.9:g.21637736A>G , CM000686.1:g.21637736A>G GRCh37
NC_000024.8:g.20097124A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000650676.1:n.238-947T>C
ENST00000400605.5:n.232-947T>C
ENST00000441139.5:n.249-947T>C
ENST00000513194.1:n.3397-952T>C
NR_002923.2:n.249-947T>C
NR_033732.1:n.249-947T>C