Canonical Allele Identifier: CA923854046
Gene: BCORP1 HGNC NCBI

Linked Data

dbSNP Id: rs2045041582
gnomAD v3: Y-19460074-A-G
gnomAD v4: Y-19460074-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19460074A>G , CM000686.2:g.19460074A>G GRCh38
NC_000024.9:g.21621960A>G , CM000686.1:g.21621960A>G GRCh37
NC_000024.8:g.20081348A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000650676.1:n.1813T>C
ENST00000400605.5:n.1807T>C
ENST00000441139.5:n.1794-708T>C
ENST00000513194.1:n.4580-708T>C
NR_002923.2:n.1794-708T>C
NR_033732.1:n.1824T>C
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