Canonical Allele Identifier: CA337396397
Gene: BCORP1 HGNC NCBI

Linked Data

dbSNP Id: rs939599331
gnomAD v3: Y-19482738-G-C
gnomAD v4: Y-19482738-G-C
MyVariant Identifiers: chrY:g.21644624G>C (hg19) chrY:g.19482738G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19482738G>C , CM000686.2:g.19482738G>C GRCh38
NC_000024.9:g.21644624G>C , CM000686.1:g.21644624G>C GRCh37
NC_000024.8:g.20104012G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000650676.1:n.112-2444C>G
ENST00000400605.5:n.106-2444C>G
ENST00000441139.5:n.123-2444C>G
ENST00000513194.1:n.2147C>G
NR_002923.2:n.123-2444C>G
NR_033732.1:n.123-2444C>G
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