Canonical Allele Identifier: CA2670843364

Gene: UGT2B15

Linked Data

• gnomAD v4: 4-68646628-CTT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.68646637_68646638del , CM000666.2:g.68646637_68646638del	GRCh38
NC_000004.11:g.69512355_69512356del , CM000666.1:g.69512355_69512356del	GRCh37
NC_000004.10:g.69194950_69194951del	NCBI36
NG_052676.1:g.29147_29148del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338206.6:c.*474_*475del MANE Select	ENSP00000341045.5:n.*474_*475del
ENST00000616841.4:c.1732+335_1732+336del	ENSP00000482004.1:n.1732+335_1732+336del
NM_001076.3:c.*474_*475del	NP_001067.2:n.*474_*475del
NM_001076.4:c.*474_*475del MANE Select	NP_001067.2:n.*474_*475del