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ClinGen Allele Registry
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Canonical Allele Identifier:
CA431957319
Community Standard Title: NM_019076.5(UGT1A8):c.765A>T (p.Thr255=)
Gene: UGT1A8
HGNC
NCBI
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000002.12:g.233618472A>T , CM000664.2:g.233618472A>T
GRCh38
NC_000002.11:g.234527118A>T , CM000664.1:g.234527118A>T
GRCh37
NC_000002.10:g.234191857A>T
NCBI36
NG_002601.2:g.33729A>T
Transcript Alleles
HGVS
Amino-acid Change
NM_019076.5:c.765A>T
MANE Select
NP_061949.3:p.Thr255=
ENST00000373450.5:c.765A>T
MANE Select
ENSP00000362549.4:p.Thr255=
NM_019076.4:c.765A>T
NP_061949.3:p.Thr255=
ENST00000373450.4:c.765A>T
ENSP00000362549.4:p.Thr255=
Search 100 bp 5'
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