Canonical Allele Identifier: CA337397672
Gene: BCORP1 HGNC NCBI

Linked Data

dbSNP Id: rs939616277
MyVariant Identifiers: chrY:g.21674367T>A (hg19) chrY:g.19512481T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19512481T>A , CM000686.2:g.19512481T>A GRCh38
NC_000024.9:g.21674367T>A , CM000686.1:g.21674367T>A GRCh37
NC_000024.8:g.20133755T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000650676.1:n.112-32187A>T
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