Canonical Allele Identifier: CA2670843641

Gene: UGT2B15

Linked Data

• gnomAD v4: 4-68646938-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.68646938T>A , CM000666.2:g.68646938T>A	GRCh38
NC_000004.11:g.69512656T>A , CM000666.1:g.69512656T>A	GRCh37
NC_000004.10:g.69195251T>A	NCBI36
NG_052676.1:g.28839A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338206.6:c.*166A>T MANE Select	ENSP00000341045.5:n.*166A>T
ENST00000338206.5:c.*166A>T	ENSP00000341045.5:n.*166A>T
ENST00000616841.4:c.1732+27A>T	ENSP00000482004.1:n.1732+27A>T
NM_001076.3:c.*166A>T	NP_001067.2:n.*166A>T
NM_001076.4:c.*166A>T MANE Select	NP_001067.2:n.*166A>T