Canonical Allele Identifier: CA431957522
Gene: UGT1A8 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.234527193A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.233618547A>G , CM000664.2:g.233618547A>G GRCh38
NC_000002.11:g.234527193A>G , CM000664.1:g.234527193A>G GRCh37
NC_000002.10:g.234191932A>G NCBI36
NG_002601.2:g.33804A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000373450.5:c.840A>G MANE Select ENSP00000362549.4:p.Gly280=
ENST00000373450.4:c.840A>G ENSP00000362549.4:p.Gly280=
NM_019076.4:c.840A>G NP_061949.3:p.Gly280=
NM_019076.5:c.840A>G MANE Select NP_061949.3:p.Gly280=