Canonical Allele Identifier: CA357085439

Gene: UGT2B15

Linked Data

• MyVariant Identifiers: chr4:g.69535864C>A (hg19) ; chr4:g.68670146C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.68670146C>A , CM000666.2:g.68670146C>A	GRCh38
NC_000004.11:g.69535864C>A , CM000666.1:g.69535864C>A	GRCh37
NC_000004.10:g.69218459C>A	NCBI36
NG_052676.1:g.5631G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338206.6:c.473G>T MANE Select	ENSP00000341045.5:p.Gly158Val
ENST00000338206.5:c.473G>T	ENSP00000341045.5:p.Gly158Val
ENST00000616841.4:c.473G>T	ENSP00000482004.1:p.Gly158Val
NM_001076.3:c.473G>T	NP_001067.2:p.Gly158Val
NM_001076.4:c.473G>T MANE Select	NP_001067.2:p.Gly158Val