Canonical Allele Identifier: CA337397967

Gene: BCORP1

Linked Data

• dbSNP Id: rs778587982
• gnomAD v3: Y-19521784-T-G
• gnomAD v4: Y-19521784-T-G
• MyVariant Identifiers: chrY:g.21683670T>G (hg19) ; chrY:g.19521784T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.19521784T>G , CM000686.2:g.19521784T>G	GRCh38
NC_000024.9:g.21683670T>G , CM000686.1:g.21683670T>G	GRCh37
NC_000024.8:g.20143058T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000650676.1:n.112-41490A>C