Canonical Allele Identifier: CA2470903593
Gene: BCORP1 HGNC NCBI

Linked Data

dbSNP Id: rs2045041551
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19460060C>T , CM000686.2:g.19460060C>T GRCh38
NC_000024.9:g.21621946C>T , CM000686.1:g.21621946C>T GRCh37
NC_000024.8:g.20081334C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000650676.1:n.1827G>A
ENST00000400605.5:n.1821G>A
ENST00000441139.5:n.1794-694G>A
ENST00000513194.1:n.4580-694G>A
NR_002923.2:n.1794-694G>A
NR_033732.1:n.1838G>A
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