Canonical Allele Identifier: CA357085322

Gene: UGT2B15

Linked Data

• MyVariant Identifiers: chr4:g.69535830A>T (hg19) ; chr4:g.68670112A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.68670112A>T , CM000666.2:g.68670112A>T	GRCh38
NC_000004.11:g.69535830A>T , CM000666.1:g.69535830A>T	GRCh37
NC_000004.10:g.69218425A>T	NCBI36
NG_052676.1:g.5665T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338206.6:c.507T>A MANE Select	ENSP00000341045.5:p.Phe169Leu
ENST00000338206.5:c.507T>A	ENSP00000341045.5:p.Phe169Leu
ENST00000616841.4:c.507T>A	ENSP00000482004.1:p.Phe169Leu
NM_001076.3:c.507T>A	NP_001067.2:p.Phe169Leu
NM_001076.4:c.507T>A MANE Select	NP_001067.2:p.Phe169Leu