Canonical Allele Identifier: CA357085035
Gene: UGT2B15 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68669981T>G , CM000666.2:g.68669981T>G GRCh38
NC_000004.11:g.69535699T>G , CM000666.1:g.69535699T>G GRCh37
NC_000004.10:g.69218294T>G NCBI36
NG_052676.1:g.5796A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.638A>C MANE Select ENSP00000341045.5:p.Lys213Thr
ENST00000338206.5:c.638A>C ENSP00000341045.5:p.Lys213Thr
ENST00000616841.4:c.638A>C ENSP00000482004.1:p.Lys213Thr
NM_001076.3:c.638A>C NP_001067.2:p.Lys213Thr
NM_001076.4:c.638A>C MANE Select NP_001067.2:p.Lys213Thr