Canonical Allele Identifier: CA337395781

Gene: BCORP1

Linked Data

• dbSNP Id: rs756914090
• gnomAD v3: Y-19466365-A-G
• gnomAD v4: Y-19466365-A-G
• MyVariant Identifiers: chrY:g.21628251A>G (hg19) ; chrY:g.19466365A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000024.10:g.19466365A>G , CM000686.2:g.19466365A>G	GRCh38
NC_000024.9:g.21628251A>G , CM000686.1:g.21628251A>G	GRCh37
NC_000024.8:g.20087639A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000650676.1:n.1660+91T>C
ENST00000400605.5:n.1654+91T>C
ENST00000441139.5:n.1671+91T>C
ENST00000513194.1:n.4579+79T>C
NR_002923.2:n.1671+91T>C
NR_033732.1:n.1671+91T>C