Canonical Allele Identifier: CA357085048
Gene: UGT2B15 HGNC NCBI

Linked Data

dbSNP Id: rs1337217493

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68669987C>T , CM000666.2:g.68669987C>T GRCh38
NC_000004.11:g.69535705C>T , CM000666.1:g.69535705C>T GRCh37
NC_000004.10:g.69218300C>T NCBI36
NG_052676.1:g.5790G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.632G>A MANE Select ENSP00000341045.5:p.Arg211Lys
ENST00000338206.5:c.632G>A ENSP00000341045.5:p.Arg211Lys
ENST00000616841.4:c.632G>A ENSP00000482004.1:p.Arg211Lys
NM_001076.3:c.632G>A NP_001067.2:p.Arg211Lys
NM_001076.4:c.632G>A MANE Select NP_001067.2:p.Arg211Lys