Canonical Allele Identifier: CA2670844558
Gene: UGT2B15 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68670175_68670177del , CM000666.2:g.68670175_68670177del GRCh38
NC_000004.11:g.69535893_69535895del , CM000666.1:g.69535893_69535895del GRCh37
NC_000004.10:g.69218488_69218490del NCBI36
NG_052676.1:g.5600_5602del

Transcript Alleles

HGVS Amino-acid change
ENST00000338206.6:c.442_444del MANE Select ENSP00000341045.5:p.Val148del
ENST00000338206.5:c.442_444del ENSP00000341045.5:p.Val148del
ENST00000616841.4:c.442_444del ENSP00000482004.1:p.Val148del
NM_001076.3:c.442_444del NP_001067.2:p.Val148del
NM_001076.4:c.442_444del MANE Select NP_001067.2:p.Val148del