Canonical Allele Identifier: CA923861447
Gene: BCORP1 HGNC NCBI

Linked Data

gnomAD v3: Y-19475892-C-T
gnomAD v4: Y-19475892-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19475892C>T , CM000686.2:g.19475892C>T GRCh38
NC_000024.9:g.21637778C>T , CM000686.1:g.21637778C>T GRCh37
NC_000024.8:g.20097166C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000650676.1:n.238-989G>A
ENST00000400605.5:n.232-989G>A
ENST00000441139.5:n.249-989G>A
ENST00000513194.1:n.3397-994G>A
NR_002923.2:n.249-989G>A
NR_033732.1:n.249-989G>A