Canonical Allele Identifier: CA1063752926

Gene: UGT2B15

Linked Data

• dbSNP Id: rs1732502196
• gnomAD v3: 4-68647168-GT-G
• gnomAD v4: 4-68647168-GT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.68647169del , CM000666.2:g.68647169del	GRCh38
NC_000004.11:g.69512887del , CM000666.1:g.69512887del	GRCh37
NC_000004.10:g.69195482del	NCBI36
NG_052676.1:g.28608del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338206.6:c.1528del MANE Select	ENSP00000341045.5:p.Thr510GlnfsTer?
ENST00000338206.5:c.1528del	ENSP00000341045.5:p.Thr510GlnfsTer?
ENST00000616841.4:c.1528del	ENSP00000482004.1:p.Thr510GlnfsTer?
NM_001076.3:c.1528del	NP_001067.2:p.Thr510GlnfsTer?
NM_001076.4:c.1528del MANE Select	NP_001067.2:p.Thr510GlnfsTer?