Canonical Allele Identifier: CA2670843754
Gene: UGT2B15 HGNC NCBI

Linked Data

gnomAD v4: 4-68647139-GC-G
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68647140del , CM000666.2:g.68647140del GRCh38
NC_000004.11:g.69512858del , CM000666.1:g.69512858del GRCh37
NC_000004.10:g.69195453del NCBI36
NG_052676.1:g.28637del

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.1557del MANE Select ENSP00000341045.5:p.Lys519AsnfsTer23
ENST00000338206.5:c.1557del ENSP00000341045.5:p.Lys519AsnfsTer23
ENST00000616841.4:c.1557del ENSP00000482004.1:p.Lys519AsnfsTer23
NM_001076.3:c.1557del NP_001067.2:p.Lys519AsnfsTer23
NM_001076.4:c.1557del MANE Select NP_001067.2:p.Lys519AsnfsTer23
Search 100 bp 5'
Search 100 bp 3'