Canonical Allele Identifier: CA357086393
Gene: UGT2B15 HGNC NCBI

Linked Data

COSMIC: COSM295053

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68670317A>G , CM000666.2:g.68670317A>G GRCh38
NC_000004.11:g.69536035A>G , CM000666.1:g.69536035A>G GRCh37
NC_000004.10:g.69218630A>G NCBI36
NG_052676.1:g.5460T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.302T>C MANE Select ENSP00000341045.5:p.Val101Ala
ENST00000338206.5:c.302T>C ENSP00000341045.5:p.Val101Ala
ENST00000616841.4:c.302T>C ENSP00000482004.1:p.Val101Ala
NM_001076.3:c.302T>C NP_001067.2:p.Val101Ala
NM_001076.4:c.302T>C MANE Select NP_001067.2:p.Val101Ala