Canonical Allele Identifier: CA98747440
Gene: UGT2B15 HGNC NCBI

Linked Data

dbSNP Id: rs549347993
gnomAD v2: 4-69512346-C-CT
gnomAD v3: 4-68646628-C-CT
gnomAD v4: 4-68646628-C-CT
MyVariant Identifiers: chr4:g.69512347_69512348insT (hg19) chr4:g.69512346_69512347insT (hg19) chr4:g.68646629_68646630insT (hg38) chr4:g.68646628_68646629insT (hg38)
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Genomic Alleles

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

Transcript Alleles

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