Canonical Allele Identifier: CA357085817
Gene: UGT2B15 HGNC NCBI

Linked Data

dbSNP Id: rs1733266208

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68670228C>T , CM000666.2:g.68670228C>T GRCh38
NC_000004.11:g.69535946C>T , CM000666.1:g.69535946C>T GRCh37
NC_000004.10:g.69218541C>T NCBI36
NG_052676.1:g.5549G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.391G>A MANE Select ENSP00000341045.5:p.Ala131Thr
ENST00000338206.5:c.391G>A ENSP00000341045.5:p.Ala131Thr
ENST00000616841.4:c.391G>A ENSP00000482004.1:p.Ala131Thr
NM_001076.3:c.391G>A NP_001067.2:p.Ala131Thr
NM_001076.4:c.391G>A MANE Select NP_001067.2:p.Ala131Thr