Canonical Allele Identifier: CA552612253
Gene: UGT2B15 HGNC NCBI

Linked Data

dbSNP Id: rs1254542091
gnomAD v2: 4-69535695-A-AT
gnomAD v4: 4-68669977-A-AT
MyVariant Identifiers: chr4:g.69535695_69535696insT (hg19) chr4:g.68669977_68669978insT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68669983dup , CM000666.2:g.68669983dup GRCh38
NC_000004.11:g.69535701dup , CM000666.1:g.69535701dup GRCh37
NC_000004.10:g.69218296dup NCBI36
NG_052676.1:g.5799dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.641dup MANE Select ENSP00000341045.5:p.Asn214LysfsTer9
ENST00000338206.5:c.641dup ENSP00000341045.5:p.Asn214LysfsTer9
ENST00000616841.4:c.641dup ENSP00000482004.1:p.Asn214LysfsTer9
NM_001076.3:c.641dup NP_001067.2:p.Asn214LysfsTer9
NM_001076.4:c.641dup MANE Select NP_001067.2:p.Asn214LysfsTer9
Search 100 bp 5'
Search 100 bp 3'