Canonical Allele Identifier: CA2578102211
Gene: UGT2B15 HGNC NCBI

Linked Data

gnomAD v4: 4-68647013-GA-G
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68647018del , CM000666.2:g.68647018del GRCh38
NC_000004.11:g.69512736del , CM000666.1:g.69512736del GRCh37
NC_000004.10:g.69195331del NCBI36
NG_052676.1:g.28763del

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.*90del MANE Select ENSP00000341045.5:n.*90del
ENST00000338206.5:c.*90del ENSP00000341045.5:n.*90del
ENST00000616841.4:c.1683del ENSP00000482004.1:n.1683del
NM_001076.3:c.*90del NP_001067.2:n.*90del
NM_001076.4:c.*90del MANE Select NP_001067.2:n.*90del
Search 100 bp 5'
Search 100 bp 3'