Canonical Allele Identifier: CA2507436525
Gene: UGT2B15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68646984del , CM000666.2:g.68646984del GRCh38
NC_000004.11:g.69512702del , CM000666.1:g.69512702del GRCh37
NC_000004.10:g.69195297del NCBI36
NG_052676.1:g.28794del

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.*121del MANE Select ENSP00000341045.5:n.*121del
ENST00000338206.5:c.*121del ENSP00000341045.5:n.*121del
ENST00000616841.4:c.1714del ENSP00000482004.1:n.1714del
NM_001076.3:c.*121del NP_001067.2:n.*121del
NM_001076.4:c.*121del MANE Select NP_001067.2:n.*121del