Canonical Allele Identifier: CA439705827

Gene: UGT2B15

Linked Data

• COSMIC: COSM3661169
• MyVariant Identifiers: chr4:g.69536330G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.68670612G>A , CM000666.2:g.68670612G>A	GRCh38
NC_000004.11:g.69536330G>A , CM000666.1:g.69536330G>A	GRCh37
NC_000004.10:g.69218925G>A	NCBI36
NG_052676.1:g.5165C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338206.6:c.7C>T MANE Select	ENSP00000341045.5:p.Leu3=
ENST00000338206.5:c.7C>T	ENSP00000341045.5:p.Leu3=
ENST00000616841.4:c.7C>T	ENSP00000482004.1:p.Leu3=
NM_001076.3:c.7C>T	NP_001067.2:p.Leu3=
NM_001076.4:c.7C>T MANE Select	NP_001067.2:p.Leu3=