Canonical Allele Identifier: CA1465820781
Gene: UGT2B15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68646753A= , CM000666.2:g.68646753A= GRCh38
NC_000004.11:g.69512471A= , CM000666.1:g.69512471A= GRCh37
NC_000004.10:g.69195066A= NCBI36
NG_052676.1:g.29024T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.*351T= MANE Select ENSP00000341045.5:n.*351T=
ENST00000338206.5:c.*351T= ENSP00000341045.5:n.*351T=
ENST00000616841.4:c.1732+212T= ENSP00000482004.1:n.1732+212T=
NM_001076.3:c.*351T= NP_001067.2:n.*351T=
NM_001076.4:c.*351T= MANE Select NP_001067.2:n.*351T=