Canonical Allele Identifier: CA880362373

Gene: BCORP1

Linked Data

• dbSNP Id: rs1479633486
• MyVariant Identifiers: chrY:g.21628721G>T (hg19) ; chrY:g.19466835G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.19466835G>T , CM000686.2:g.19466835G>T	GRCh38
NC_000024.9:g.21628721G>T , CM000686.1:g.21628721G>T	GRCh37
NC_000024.8:g.20088109G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650676.1:n.1281C>A
ENST00000400605.5:n.1275C>A
ENST00000441139.5:n.1292C>A
ENST00000513194.1:n.4316-128C>A
NR_002923.2:n.1292C>A
NR_033732.1:n.1292C>A