Canonical Allele Identifier: CA2670843404

Gene: UGT2B15

Linked Data

• gnomAD v4: 4-68646729-A-ATTTTT

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.68646737_68646741dup , CM000666.2:g.68646737_68646741dup	GRCh38
NC_000004.11:g.69512455_69512459dup , CM000666.1:g.69512455_69512459dup	GRCh37
NC_000004.10:g.69195050_69195054dup	NCBI36
NG_052676.1:g.29043_29047dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338206.6:c.*370_*374dup MANE Select	ENSP00000341045.5:n.*370_*374dup
ENST00000338206.5:c.*370_*374dup	ENSP00000341045.5:n.*370_*374dup
ENST00000616841.4:c.1732+231_1732+235dup	ENSP00000482004.1:n.1732+231_1732+235dup
NM_001076.3:c.*370_*374dup	NP_001067.2:n.*370_*374dup
NM_001076.4:c.*370_*374dup MANE Select	NP_001067.2:n.*370_*374dup