Canonical Allele Identifier: CA337396149

Gene: BCORP1

Linked Data

• dbSNP Id: rs1017661826
• MyVariant Identifiers: chrY:g.21637747C>G (hg19) ; chrY:g.19475861C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.19475861C>G , CM000686.2:g.19475861C>G	GRCh38
NC_000024.9:g.21637747C>G , CM000686.1:g.21637747C>G	GRCh37
NC_000024.8:g.20097135C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650676.1:n.238-958G>C
ENST00000400605.5:n.232-958G>C
ENST00000441139.5:n.249-958G>C
ENST00000513194.1:n.3397-963G>C
NR_002923.2:n.249-958G>C
NR_033732.1:n.249-958G>C