Canonical Allele Identifier: CA2470906981
Gene: BCORP1 HGNC NCBI

Linked Data

dbSNP Id: rs2045089814
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19521805C>A , CM000686.2:g.19521805C>A GRCh38
NC_000024.9:g.21683691C>A , CM000686.1:g.21683691C>A GRCh37
NC_000024.8:g.20143079C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000650676.1:n.112-41511G>T
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