Canonical Allele Identifier: CA439934725

Gene: UGT2B15

Linked Data

• MyVariant Identifiers: chr4:g.69512924G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.68647206G>A , CM000666.2:g.68647206G>A	GRCh38
NC_000004.11:g.69512924G>A , CM000666.1:g.69512924G>A	GRCh37
NC_000004.10:g.69195519G>A	NCBI36
NG_052676.1:g.28571C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338206.6:c.1491C>T MANE Select	ENSP00000341045.5:p.Phe497=
ENST00000338206.5:c.1491C>T	ENSP00000341045.5:p.Phe497=
ENST00000616841.4:c.1491C>T	ENSP00000482004.1:p.Phe497=
NM_001076.3:c.1491C>T	NP_001067.2:p.Phe497=
NM_001076.4:c.1491C>T MANE Select	NP_001067.2:p.Phe497=