Canonical Allele Identifier: CA337396147
Gene: BCORP1 HGNC NCBI

Linked Data

dbSNP Id: rs1006232636
gnomAD v3: Y-19475847-T-C
gnomAD v4: Y-19475847-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19475847T>C , CM000686.2:g.19475847T>C GRCh38
NC_000024.9:g.21637733T>C , CM000686.1:g.21637733T>C GRCh37
NC_000024.8:g.20097121T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000650676.1:n.238-944A>G
ENST00000400605.5:n.232-944A>G
ENST00000441139.5:n.249-944A>G
ENST00000513194.1:n.3397-949A>G
NR_002923.2:n.249-944A>G
NR_033732.1:n.249-944A>G