Canonical Allele Identifier: CA2177648
Gene: UGT1A8 HGNC NCBI

Linked Data

dbSNP Id: rs147191221

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.233618538C>A , CM000664.2:g.233618538C>A GRCh38
NC_000002.11:g.234527184C>A , CM000664.1:g.234527184C>A GRCh37
NC_000002.10:g.234191923C>A NCBI36
NG_002601.2:g.33795C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000373450.5:c.831C>A MANE Select ENSP00000362549.4:p.Cys277Ter
ENST00000373450.4:c.831C>A ENSP00000362549.4:p.Cys277Ter
NM_019076.4:c.831C>A NP_061949.3:p.Cys277Ter
NM_019076.5:c.831C>A MANE Select NP_061949.3:p.Cys277Ter