Canonical Allele Identifier: CA552177722
Gene: UGT2B15 HGNC NCBI

Linked Data

dbSNP Id: rs549347993
gnomAD v2: 4-69512346-CT-C
gnomAD v3: 4-68646628-CT-C
gnomAD v4: 4-68646628-CT-C
MyVariant Identifiers: chr4:g.69512347del (hg19) chr4:g.68646629del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68646638del , CM000666.2:g.68646638del GRCh38
NC_000004.11:g.69512356del , CM000666.1:g.69512356del GRCh37
NC_000004.10:g.69194951del NCBI36
NG_052676.1:g.29148del

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.*475del MANE Select ENSP00000341045.5:n.*475del
ENST00000616841.4:c.1732+336del ENSP00000482004.1:n.1732+336del
NM_001076.3:c.*475del NP_001067.2:n.*475del
NM_001076.4:c.*475del MANE Select NP_001067.2:n.*475del
Search 100 bp 5'
Search 100 bp 3'