Canonical Allele Identifier: CA351073425
Gene: UGT1A8 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.234527095A>C (hg19) chr2:g.233618449A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.233618449A>C , CM000664.2:g.233618449A>C GRCh38
NC_000002.11:g.234527095A>C , CM000664.1:g.234527095A>C GRCh37
NC_000002.10:g.234191834A>C NCBI36
NG_002601.2:g.33706A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000373450.5:c.742A>C MANE Select ENSP00000362549.4:p.Thr248Pro
ENST00000373450.4:c.742A>C ENSP00000362549.4:p.Thr248Pro
NM_019076.4:c.742A>C NP_061949.3:p.Thr248Pro
NM_019076.5:c.742A>C MANE Select NP_061949.3:p.Thr248Pro
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