Canonical Allele Identifier: CA1465820933
Gene: UGT2B15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68647010C= , CM000666.2:g.68647010C= GRCh38
NC_000004.11:g.69512728C= , CM000666.1:g.69512728C= GRCh37
NC_000004.10:g.69195323C= NCBI36
NG_052676.1:g.28767G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.*94G= MANE Select ENSP00000341045.5:n.*94G=
ENST00000338206.5:c.*94G= ENSP00000341045.5:n.*94G=
ENST00000616841.4:c.1687G= ENSP00000482004.1:n.1687G=
NM_001076.3:c.*94G= NP_001067.2:n.*94G=
NM_001076.4:c.*94G= MANE Select NP_001067.2:n.*94G=