Canonical Allele Identifier: CA2670843756

Gene: UGT2B15

Linked Data

• gnomAD v4: 4-68647180-AT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.68647181del , CM000666.2:g.68647181del	GRCh38
NC_000004.11:g.69512899del , CM000666.1:g.69512899del	GRCh37
NC_000004.10:g.69195494del	NCBI36
NG_052676.1:g.28596del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338206.6:c.1516del MANE Select	ENSP00000341045.5:p.Ile506TyrfsTer?
ENST00000338206.5:c.1516del	ENSP00000341045.5:p.Ile506TyrfsTer?
ENST00000616841.4:c.1516del	ENSP00000482004.1:p.Ile506TyrfsTer?
NM_001076.3:c.1516del	NP_001067.2:p.Ile506TyrfsTer?
NM_001076.4:c.1516del MANE Select	NP_001067.2:p.Ile506TyrfsTer?