Canonical Allele Identifier: CA2177647
Gene: UGT1A8 HGNC NCBI

Linked Data

dbSNP Id: rs147191221

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000373450.5:c.831C>T MANE Select ENSP00000362549.4:p.Cys277=
ENST00000373450.4:c.831C>T ENSP00000362549.4:p.Cys277=
NM_019076.4:c.831C>T NP_061949.3:p.Cys277=
NM_019076.5:c.831C>T MANE Select NP_061949.3:p.Cys277=