Canonical Allele Identifier: CA923861413
Gene: BCORP1 HGNC NCBI

Linked Data

gnomAD v3: Y-19475855-T-C
gnomAD v4: Y-19475855-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19475855T>C , CM000686.2:g.19475855T>C GRCh38
NC_000024.9:g.21637741T>C , CM000686.1:g.21637741T>C GRCh37
NC_000024.8:g.20097129T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000650676.1:n.238-952A>G
ENST00000400605.5:n.232-952A>G
ENST00000441139.5:n.249-952A>G
ENST00000513194.1:n.3397-957A>G
NR_002923.2:n.249-952A>G
NR_033732.1:n.249-952A>G