Canonical Allele Identifier: CA357083098
Gene: UGT2B15 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68647205G>C , CM000666.2:g.68647205G>C GRCh38
NC_000004.11:g.69512923G>C , CM000666.1:g.69512923G>C GRCh37
NC_000004.10:g.69195518G>C NCBI36
NG_052676.1:g.28572C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.1492C>G MANE Select ENSP00000341045.5:p.Leu498Val
ENST00000338206.5:c.1492C>G ENSP00000341045.5:p.Leu498Val
ENST00000616841.4:c.1492C>G ENSP00000482004.1:p.Leu498Val
NM_001076.3:c.1492C>G NP_001067.2:p.Leu498Val
NM_001076.4:c.1492C>G MANE Select NP_001067.2:p.Leu498Val