Canonical Allele Identifier: CA431957584
Gene: UGT1A8 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.234527205T>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.233618559T>G , CM000664.2:g.233618559T>G GRCh38
NC_000002.11:g.234527205T>G , CM000664.1:g.234527205T>G GRCh37
NC_000002.10:g.234191944T>G NCBI36
NG_002601.2:g.33816T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000373450.5:c.852T>G MANE Select ENSP00000362549.4:p.Pro284=
ENST00000373450.4:c.852T>G ENSP00000362549.4:p.Pro284=
NM_019076.4:c.852T>G NP_061949.3:p.Pro284=
NM_019076.5:c.852T>G MANE Select NP_061949.3:p.Pro284=
Search 100 bp 5'
Search 100 bp 3'