Canonical Allele Identifier: CA923854017
Gene: BCORP1 HGNC NCBI

Linked Data

dbSNP Id: rs2045041499
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19460041G>T , CM000686.2:g.19460041G>T GRCh38
NC_000024.9:g.21621927G>T , CM000686.1:g.21621927G>T GRCh37
NC_000024.8:g.20081315G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000650676.1:n.1846C>A
ENST00000400605.5:n.1840C>A
ENST00000441139.5:n.1794-675C>A
ENST00000513194.1:n.4580-675C>A
NR_002923.2:n.1794-675C>A
NR_033732.1:n.1857C>A
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