Canonical Allele Identifier: CA1465820911
Gene: UGT2B15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68646969T= , CM000666.2:g.68646969T= GRCh38
NC_000004.11:g.69512687T= , CM000666.1:g.69512687T= GRCh37
NC_000004.10:g.69195282T= NCBI36
NG_052676.1:g.28808A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.*135A= MANE Select ENSP00000341045.5:n.*135A=
ENST00000338206.5:c.*135A= ENSP00000341045.5:n.*135A=
ENST00000616841.4:c.1728A= ENSP00000482004.1:n.1728A=
NM_001076.3:c.*135A= NP_001067.2:n.*135A=
NM_001076.4:c.*135A= MANE Select NP_001067.2:n.*135A=