Canonical Allele Identifier: CA337396416
Gene: BCORP1 HGNC NCBI

Linked Data

dbSNP Id: rs1015983929
MyVariant Identifiers: chrY:g.21645079G>C (hg19) chrY:g.19483193G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19483193G>C , CM000686.2:g.19483193G>C GRCh38
NC_000024.9:g.21645079G>C , CM000686.1:g.21645079G>C GRCh37
NC_000024.8:g.20104467G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000650676.1:n.112-2899C>G
ENST00000400605.5:n.106-2899C>G
ENST00000441139.5:n.123-2899C>G
ENST00000513194.1:n.1692C>G
NR_002923.2:n.123-2899C>G
NR_033732.1:n.123-2899C>G
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