Canonical Allele Identifier: CA923861439
Gene: BCORP1 HGNC NCBI

Linked Data

dbSNP Id: rs2124147180
gnomAD v3: Y-19475886-A-C
gnomAD v4: Y-19475886-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19475886A>C , CM000686.2:g.19475886A>C GRCh38
NC_000024.9:g.21637772A>C , CM000686.1:g.21637772A>C GRCh37
NC_000024.8:g.20097160A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000650676.1:n.238-983T>G
ENST00000400605.5:n.232-983T>G
ENST00000441139.5:n.249-983T>G
ENST00000513194.1:n.3397-988T>G
NR_002923.2:n.249-983T>G
NR_033732.1:n.249-983T>G