Canonical Allele Identifier: CA351073429
Gene: UGT1A8 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.234527096C>T (hg19) chr2:g.233618450C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.233618450C>T , CM000664.2:g.233618450C>T GRCh38
NC_000002.11:g.234527096C>T , CM000664.1:g.234527096C>T GRCh37
NC_000002.10:g.234191835C>T NCBI36
NG_002601.2:g.33707C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000373450.5:c.743C>T MANE Select ENSP00000362549.4:p.Thr248Ile
ENST00000373450.4:c.743C>T ENSP00000362549.4:p.Thr248Ile
NM_019076.4:c.743C>T NP_061949.3:p.Thr248Ile
NM_019076.5:c.743C>T MANE Select NP_061949.3:p.Thr248Ile
Search 100 bp 5'
Search 100 bp 3'