Canonical Allele Identifier: CA357083075
Gene: UGT2B15 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68647192A>G , CM000666.2:g.68647192A>G GRCh38
NC_000004.11:g.69512910A>G , CM000666.1:g.69512910A>G GRCh37
NC_000004.10:g.69195505A>G NCBI36
NG_052676.1:g.28585T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.1505T>C MANE Select ENSP00000341045.5:p.Val502Ala
ENST00000338206.5:c.1505T>C ENSP00000341045.5:p.Val502Ala
ENST00000616841.4:c.1505T>C ENSP00000482004.1:p.Val502Ala
NM_001076.3:c.1505T>C NP_001067.2:p.Val502Ala
NM_001076.4:c.1505T>C MANE Select NP_001067.2:p.Val502Ala