Canonical Allele Identifier: CA1335825644
Gene: UGT1A8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.233618541T= , CM000664.2:g.233618541T= GRCh38
NC_000002.11:g.234527187T= , CM000664.1:g.234527187T= GRCh37
NC_000002.10:g.234191926T= NCBI36
NG_002601.2:g.33798T=

Transcript Alleles

HGVS Amino-acid change
ENST00000373450.5:c.834T= MANE Select ENSP00000362549.4:p.His278=
ENST00000373450.4:c.834T= ENSP00000362549.4:p.His278=
NM_019076.4:c.834T= NP_061949.3:p.His278=
NM_019076.5:c.834T= MANE Select NP_061949.3:p.His278=