Canonical Allele Identifier: CA2670843363

Gene: UGT2B15

Linked Data

• gnomAD v4: 4-68646628-C-CTTT

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.68646636_68646638dup , CM000666.2:g.68646636_68646638dup	GRCh38
NC_000004.11:g.69512354_69512356dup , CM000666.1:g.69512354_69512356dup	GRCh37
NC_000004.10:g.69194949_69194951dup	NCBI36
NG_052676.1:g.29146_29148dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338206.6:c.*473_*475dup MANE Select	ENSP00000341045.5:n.*473_*475dup
ENST00000616841.4:c.1732+334_1732+336dup	ENSP00000482004.1:n.1732+334_1732+336dup
NM_001076.3:c.*473_*475dup	NP_001067.2:n.*473_*475dup
NM_001076.4:c.*473_*475dup MANE Select	NP_001067.2:n.*473_*475dup