Canonical Allele Identifier: CA431957319
Gene: UGT1A8 HGNC NCBI

Linked Data

dbSNP Id: rs1042605

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.233618472A>T , CM000664.2:g.233618472A>T GRCh38
NC_000002.11:g.234527118A>T , CM000664.1:g.234527118A>T GRCh37
NC_000002.10:g.234191857A>T NCBI36
NG_002601.2:g.33729A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000373450.5:c.765A>T MANE Select ENSP00000362549.4:p.Thr255=
ENST00000373450.4:c.765A>T ENSP00000362549.4:p.Thr255=
NM_019076.4:c.765A>T NP_061949.3:p.Thr255=
NM_019076.5:c.765A>T MANE Select NP_061949.3:p.Thr255=