Canonical Allele Identifier: CA1465820987
Gene: UGT2B15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68647100A= , CM000666.2:g.68647100A= GRCh38
NC_000004.11:g.69512818A= , CM000666.1:g.69512818A= GRCh37
NC_000004.10:g.69195413A= NCBI36
NG_052676.1:g.28677T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.*4T= MANE Select ENSP00000341045.5:n.*4T=
ENST00000338206.5:c.*4T= ENSP00000341045.5:n.*4T=
ENST00000616841.4:c.1597T= ENSP00000482004.1:n.1597T=
NM_001076.3:c.*4T= NP_001067.2:n.*4T=
NM_001076.4:c.*4T= MANE Select NP_001067.2:n.*4T=