Canonical Allele Identifier: CA2844466261
Gene: BCORP1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19503514A>G , CM000686.2:g.19503514A>G GRCh38
NC_000024.9:g.21665400A>G , CM000686.1:g.21665400A>G GRCh37
NC_000024.8:g.20124788A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000650676.1:n.112-23220T>C
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