Canonical Allele Identifier: CA2670843529

Gene: UGT2B15

Linked Data

• gnomAD v4: 4-68646866-A-AATGT

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.68646866_68646867insATGT , CM000666.2:g.68646866_68646867insATGT	GRCh38
NC_000004.11:g.69512584_69512585insATGT , CM000666.1:g.69512584_69512585insATGT	GRCh37
NC_000004.10:g.69195179_69195180insATGT	NCBI36
NG_052676.1:g.28910_28911insACAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338206.6:c.*237_*238insACAT MANE Select	ENSP00000341045.5:n.*237_*238insACAT
ENST00000338206.5:c.*237_*238insACAT	ENSP00000341045.5:n.*237_*238insACAT
ENST00000616841.4:c.1732+98_1732+99insACAT	ENSP00000482004.1:n.1732+98_1732+99insACAT
NM_001076.3:c.*237_*238insACAT	NP_001067.2:n.*237_*238insACAT
NM_001076.4:c.*237_*238insACAT MANE Select	NP_001067.2:n.*237_*238insACAT