Canonical Allele Identifier: CA1465794469
Gene: UGT2B15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68670374G= , CM000666.2:g.68670374G= GRCh38
NC_000004.11:g.69536092G= , CM000666.1:g.69536092G= GRCh37
NC_000004.10:g.69218687G= NCBI36
NG_052676.1:g.5403C=

Transcript Alleles

HGVS Amino-acid change
ENST00000338206.6:c.245C= MANE Select ENSP00000341045.5:p.Thr82=
ENST00000338206.5:c.245C= ENSP00000341045.5:p.Thr82=
ENST00000616841.4:c.245C= ENSP00000482004.1:p.Thr82=
NM_001076.3:c.245C= NP_001067.2:p.Thr82=
NM_001076.4:c.245C= MANE Select NP_001067.2:p.Thr82=