Canonical Allele Identifier: CA351074227
Gene: UGT1A8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.233618546G>C , CM000664.2:g.233618546G>C GRCh38
NC_000002.11:g.234527192G>C , CM000664.1:g.234527192G>C GRCh37
NC_000002.10:g.234191931G>C NCBI36
NG_002601.2:g.33803G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000373450.5:c.839G>C MANE Select ENSP00000362549.4:p.Gly280Ala
ENST00000373450.4:c.839G>C ENSP00000362549.4:p.Gly280Ala
NM_019076.4:c.839G>C NP_061949.3:p.Gly280Ala
NM_019076.5:c.839G>C MANE Select NP_061949.3:p.Gly280Ala