Canonical Allele Identifier: CA1465820836
Gene: UGT2B15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68646827C= , CM000666.2:g.68646827C= GRCh38
NC_000004.11:g.69512545C= , CM000666.1:g.69512545C= GRCh37
NC_000004.10:g.69195140C= NCBI36
NG_052676.1:g.28950G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.*277G= MANE Select ENSP00000341045.5:n.*277G=
ENST00000338206.5:c.*277G= ENSP00000341045.5:n.*277G=
ENST00000616841.4:c.1732+138G= ENSP00000482004.1:n.1732+138G=
NM_001076.3:c.*277G= NP_001067.2:n.*277G=
NM_001076.4:c.*277G= MANE Select NP_001067.2:n.*277G=