Canonical Allele Identifier: CA1335825595

Gene: UGT1A8

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.233618448C= , CM000664.2:g.233618448C=	GRCh38
NC_000002.11:g.234527094C= , CM000664.1:g.234527094C=	GRCh37
NC_000002.10:g.234191833C=	NCBI36
NG_002601.2:g.33705C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000373450.5:c.741C= MANE Select	ENSP00000362549.4:p.His247=
ENST00000373450.4:c.741C=	ENSP00000362549.4:p.His247=
NM_019076.4:c.741C=	NP_061949.3:p.His247=
NM_019076.5:c.741C= MANE Select	NP_061949.3:p.His247=