Canonical Allele Identifier: CA1465820979
Gene: UGT2B15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68647092C= , CM000666.2:g.68647092C= GRCh38
NC_000004.11:g.69512810C= , CM000666.1:g.69512810C= GRCh37
NC_000004.10:g.69195405C= NCBI36
NG_052676.1:g.28685G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.*12G= MANE Select ENSP00000341045.5:n.*12G=
ENST00000338206.5:c.*12G= ENSP00000341045.5:n.*12G=
ENST00000616841.4:c.1605G= ENSP00000482004.1:n.1605G=
NM_001076.3:c.*12G= NP_001067.2:n.*12G=
NM_001076.4:c.*12G= MANE Select NP_001067.2:n.*12G=