Canonical Allele Identifier: CA1465794221
Gene: UGT2B15 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68670234_68670236delinsTAC , CM000666.2:g.68670234_68670236delinsTAC GRCh38
NC_000004.11:g.69535952_69535954delinsTAC , CM000666.1:g.69535952_69535954delinsTAC GRCh37
NC_000004.10:g.69218547_69218549delinsTAC NCBI36
NG_052676.1:g.5541_5543delinsGTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.383_385delinsGTA MANE Select ENSP00000341045.5:p.Cys128=
ENST00000338206.5:c.383_385delinsGTA ENSP00000341045.5:p.Cys128=
ENST00000616841.4:c.383_385delinsGTA ENSP00000482004.1:p.Cys128=
NM_001076.3:c.383_385delinsGTA NP_001067.2:p.Cys128=
NM_001076.4:c.383_385delinsGTA MANE Select NP_001067.2:p.Cys128=
Search 100 bp 5'
Search 100 bp 3'