Canonical Allele Identifier: CA357085157
Gene: UGT2B15 HGNC NCBI

Linked Data

dbSNP Id: rs1733255975

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68670032G>T , CM000666.2:g.68670032G>T GRCh38
NC_000004.11:g.69535750G>T , CM000666.1:g.69535750G>T GRCh37
NC_000004.10:g.69218345G>T NCBI36
NG_052676.1:g.5745C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.587C>A MANE Select ENSP00000341045.5:p.Pro196His
ENST00000338206.5:c.587C>A ENSP00000341045.5:p.Pro196His
ENST00000616841.4:c.587C>A ENSP00000482004.1:p.Pro196His
NM_001076.3:c.587C>A NP_001067.2:p.Pro196His
NM_001076.4:c.587C>A MANE Select NP_001067.2:p.Pro196His