Canonical Allele Identifier: CA337397668
Gene: BCORP1 HGNC NCBI

Linked Data

dbSNP Id: rs980979786
MyVariant Identifiers: chrY:g.21674291G>A (hg19) chrY:g.19512405G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19512405G>A , CM000686.2:g.19512405G>A GRCh38
NC_000024.9:g.21674291G>A , CM000686.1:g.21674291G>A GRCh37
NC_000024.8:g.20133679G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000650676.1:n.112-32111C>T
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