Canonical Allele Identifier: CA439934687

Gene: UGT2B15

Linked Data

• MyVariant Identifiers: chr4:g.69512873C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.68647155C>G , CM000666.2:g.68647155C>G	GRCh38
NC_000004.11:g.69512873C>G , CM000666.1:g.69512873C>G	GRCh37
NC_000004.10:g.69195468C>G	NCBI36
NG_052676.1:g.28622G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338206.6:c.1542G>C MANE Select	ENSP00000341045.5:p.Leu514=
ENST00000338206.5:c.1542G>C	ENSP00000341045.5:p.Leu514=
ENST00000616841.4:c.1542G>C	ENSP00000482004.1:p.Leu514=
NM_001076.3:c.1542G>C	NP_001067.2:p.Leu514=
NM_001076.4:c.1542G>C MANE Select	NP_001067.2:p.Leu514=