Canonical Allele Identifier: CA357086598
Gene: UGT2B15 HGNC NCBI

Linked Data

gnomAD v4: 4-68670351-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68670351G>T , CM000666.2:g.68670351G>T GRCh38
NC_000004.11:g.69536069G>T , CM000666.1:g.69536069G>T GRCh37
NC_000004.10:g.69218664G>T NCBI36
NG_052676.1:g.5426C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.268C>A MANE Select ENSP00000341045.5:p.Leu90Ile
ENST00000338206.5:c.268C>A ENSP00000341045.5:p.Leu90Ile
ENST00000616841.4:c.268C>A ENSP00000482004.1:p.Leu90Ile
NM_001076.3:c.268C>A NP_001067.2:p.Leu90Ile
NM_001076.4:c.268C>A MANE Select NP_001067.2:p.Leu90Ile