Canonical Allele Identifier: CA1465820719

Gene: UGT2B15

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.68646674C= , CM000666.2:g.68646674C=	GRCh38
NC_000004.11:g.69512392C= , CM000666.1:g.69512392C=	GRCh37
NC_000004.10:g.69194987C=	NCBI36
NG_052676.1:g.29103G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338206.6:c.*430G= MANE Select	ENSP00000341045.5:n.*430G=
ENST00000338206.5:c.*430G=	ENSP00000341045.5:n.*430G=
ENST00000616841.4:c.1732+291G=	ENSP00000482004.1:n.1732+291G=
NM_001076.3:c.*430G=	NP_001067.2:n.*430G=
NM_001076.4:c.*430G= MANE Select	NP_001067.2:n.*430G=