Canonical Allele Identifier: CA337396415

Gene: BCORP1

Linked Data

• dbSNP Id: rs1004561084
• gnomAD v3: Y-19483170-T-C
• gnomAD v4: Y-19483170-T-C
• MyVariant Identifiers: chrY:g.21645056T>C (hg19) ; chrY:g.19483170T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.19483170T>C , CM000686.2:g.19483170T>C	GRCh38
NC_000024.9:g.21645056T>C , CM000686.1:g.21645056T>C	GRCh37
NC_000024.8:g.20104444T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000650676.1:n.112-2876A>G
ENST00000400605.5:n.106-2876A>G
ENST00000441139.5:n.123-2876A>G
ENST00000513194.1:n.1715A>G
NR_002923.2:n.123-2876A>G
NR_033732.1:n.123-2876A>G