Canonical Allele Identifier: CA1465794828
Gene: UGT2B15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68670565A= , CM000666.2:g.68670565A= GRCh38
NC_000004.11:g.69536283A= , CM000666.1:g.69536283A= GRCh37
NC_000004.10:g.69218878A= NCBI36
NG_052676.1:g.5212T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.54T= MANE Select ENSP00000341045.5:p.Phe18=
ENST00000338206.5:c.54T= ENSP00000341045.5:p.Phe18=
ENST00000616841.4:c.54T= ENSP00000482004.1:p.Phe18=
NM_001076.3:c.54T= NP_001067.2:p.Phe18=
NM_001076.4:c.54T= MANE Select NP_001067.2:p.Phe18=