Canonical Allele Identifier: CA351074185
Gene: UGT1A8 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.234527187T>A (hg19) chr2:g.233618541T>A (hg38)
JSON-LD

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000373450.5:c.834T>A MANE Select ENSP00000362549.4:p.His278Gln
ENST00000373450.4:c.834T>A ENSP00000362549.4:p.His278Gln
NM_019076.4:c.834T>A NP_061949.3:p.His278Gln
NM_019076.5:c.834T>A MANE Select NP_061949.3:p.His278Gln
Search 100 bp 5'
Search 100 bp 3'