Canonical Allele Identifier: CA2177649
Gene: UGT1A8 HGNC NCBI

Linked Data

dbSNP Id: rs375239720

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.233618540A>G , CM000664.2:g.233618540A>G GRCh38
NC_000002.11:g.234527186A>G , CM000664.1:g.234527186A>G GRCh37
NC_000002.10:g.234191925A>G NCBI36
NG_002601.2:g.33797A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000373450.5:c.833A>G MANE Select ENSP00000362549.4:p.His278Arg
ENST00000373450.4:c.833A>G ENSP00000362549.4:p.His278Arg
NM_019076.4:c.833A>G NP_061949.3:p.His278Arg
NM_019076.5:c.833A>G MANE Select NP_061949.3:p.His278Arg