Canonical Allele Identifier: CA357085805
Gene: UGT2B15 HGNC NCBI

Linked Data

gnomAD v4: 4-68670225-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68670225C>A , CM000666.2:g.68670225C>A GRCh38
NC_000004.11:g.69535943C>A , CM000666.1:g.69535943C>A GRCh37
NC_000004.10:g.69218538C>A NCBI36
NG_052676.1:g.5552G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.394G>T MANE Select ENSP00000341045.5:p.Val132Phe
ENST00000338206.5:c.394G>T ENSP00000341045.5:p.Val132Phe
ENST00000616841.4:c.394G>T ENSP00000482004.1:p.Val132Phe
NM_001076.3:c.394G>T NP_001067.2:p.Val132Phe
NM_001076.4:c.394G>T MANE Select NP_001067.2:p.Val132Phe