Canonical Allele Identifier: CA797794362
Gene: UGT2B15 HGNC NCBI

Linked Data

dbSNP Id: rs1237092828
gnomAD v3: 4-68669880-A-T
gnomAD v4: 4-68669880-A-T
MyVariant Identifiers: chr4:g.69535598A>T (hg19) chr4:g.68669880A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68669880A>T , CM000666.2:g.68669880A>T GRCh38
NC_000004.11:g.69535598A>T , CM000666.1:g.69535598A>T GRCh37
NC_000004.10:g.69218193A>T NCBI36
NG_052676.1:g.5897T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.724+15T>A MANE Select ENSP00000341045.5:n.724+15T>A
ENST00000338206.5:c.724+15T>A ENSP00000341045.5:n.724+15T>A
ENST00000616841.4:c.724+15T>A ENSP00000482004.1:n.724+15T>A
NM_001076.3:c.724+15T>A NP_001067.2:n.724+15T>A
NM_001076.4:c.724+15T>A MANE Select NP_001067.2:n.724+15T>A
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