Canonical Allele Identifier: CA357082933
Gene: UGT2B15 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68647123T>G , CM000666.2:g.68647123T>G GRCh38
NC_000004.11:g.69512841T>G , CM000666.1:g.69512841T>G GRCh37
NC_000004.10:g.69195436T>G NCBI36
NG_052676.1:g.28654A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.1574A>C MANE Select ENSP00000341045.5:p.Lys525Thr
ENST00000338206.5:c.1574A>C ENSP00000341045.5:p.Lys525Thr
ENST00000616841.4:c.1574A>C ENSP00000482004.1:p.Lys525Thr
NM_001076.3:c.1574A>C NP_001067.2:p.Lys525Thr
NM_001076.4:c.1574A>C MANE Select NP_001067.2:p.Lys525Thr