Canonical Allele Identifier: CA923854029
Gene: BCORP1 HGNC NCBI

Linked Data

gnomAD v3: Y-19460059-G-C
gnomAD v4: Y-19460059-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19460059G>C , CM000686.2:g.19460059G>C GRCh38
NC_000024.9:g.21621945G>C , CM000686.1:g.21621945G>C GRCh37
NC_000024.8:g.20081333G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000650676.1:n.1828C>G
ENST00000400605.5:n.1822C>G
ENST00000441139.5:n.1794-693C>G
ENST00000513194.1:n.4580-693C>G
NR_002923.2:n.1794-693C>G
NR_033732.1:n.1839C>G
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