Canonical Allele Identifier: CA2670844556
Gene: UGT2B15 HGNC NCBI

Linked Data

gnomAD v4: 4-68670014-AATTCTGACATAACAACAGGTACATAGGAAGGAGGGAACAGAAATCCTCCACC-A
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68670020_68670071del , CM000666.2:g.68670020_68670071del GRCh38
NC_000004.11:g.69535738_69535789del , CM000666.1:g.69535738_69535789del GRCh37
NC_000004.10:g.69218333_69218384del NCBI36
NG_052676.1:g.5711_5762del

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.553_604del MANE Select ENSP00000341045.5:p.Gly185Ter
ENST00000338206.5:c.553_604del ENSP00000341045.5:p.Gly185Ter
ENST00000616841.4:c.553_604del ENSP00000482004.1:p.Gly185Ter
NM_001076.3:c.553_604del NP_001067.2:p.Gly185Ter
NM_001076.4:c.553_604del MANE Select NP_001067.2:p.Gly185Ter
Search 100 bp 5'
Search 100 bp 3'