Canonical Allele Identifier: CA1335825594
Gene: UGT1A8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.233618445C= , CM000664.2:g.233618445C= GRCh38
NC_000002.11:g.234527091C= , CM000664.1:g.234527091C= GRCh37
NC_000002.10:g.234191830C= NCBI36
NG_002601.2:g.33702C=

Transcript Alleles

HGVS Amino-acid change
ENST00000373450.5:c.738C= MANE Select ENSP00000362549.4:p.Ser246=
ENST00000373450.4:c.738C= ENSP00000362549.4:p.Ser246=
NM_019076.4:c.738C= NP_061949.3:p.Ser246=
NM_019076.5:c.738C= MANE Select NP_061949.3:p.Ser246=