Canonical Allele Identifier: CA2670843642
Gene: UGT2B15 HGNC NCBI

Linked Data

gnomAD v4: 4-68646938-TA-T
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68646941del , CM000666.2:g.68646941del GRCh38
NC_000004.11:g.69512659del , CM000666.1:g.69512659del GRCh37
NC_000004.10:g.69195254del NCBI36
NG_052676.1:g.28838del

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.*165del MANE Select ENSP00000341045.5:n.*165del
ENST00000338206.5:c.*165del ENSP00000341045.5:n.*165del
ENST00000616841.4:c.1732+26del ENSP00000482004.1:n.1732+26del
NM_001076.3:c.*165del NP_001067.2:n.*165del
NM_001076.4:c.*165del MANE Select NP_001067.2:n.*165del
Search 100 bp 5'
Search 100 bp 3'