Canonical Allele Identifier: CA337398551
Gene: BCORP1 HGNC NCBI

Linked Data

dbSNP Id: rs375151448
gnomAD v3: Y-19544474-A-T
gnomAD v4: Y-19544474-A-T
MyVariant Identifiers: chrY:g.21706360A>T (hg19) chrY:g.19544474A>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.19544474A>T , CM000686.2:g.19544474A>T GRCh38
NC_000024.9:g.21706360A>T , CM000686.1:g.21706360A>T GRCh37
NC_000024.8:g.20165748A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000650676.1:n.111+22508T>A
Search 100 bp 5'
Search 100 bp 3'