Canonical Allele Identifier: CA1335825646
Gene: UGT1A8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.233618545G= , CM000664.2:g.233618545G= GRCh38
NC_000002.11:g.234527191G= , CM000664.1:g.234527191G= GRCh37
NC_000002.10:g.234191930G= NCBI36
NG_002601.2:g.33802G=

Transcript Alleles

HGVS Amino-acid change
ENST00000373450.5:c.838G= MANE Select ENSP00000362549.4:p.Gly280=
ENST00000373450.4:c.838G= ENSP00000362549.4:p.Gly280=
NM_019076.4:c.838G= NP_061949.3:p.Gly280=
NM_019076.5:c.838G= MANE Select NP_061949.3:p.Gly280=