Canonical Allele Identifier: CA439705736
Gene: UGT2B15 HGNC NCBI

Linked Data

dbSNP Id: rs1733254324
gnomAD v4: 4-68669989-C-T
MyVariant Identifiers: chr4:g.69535707C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68669989C>T , CM000666.2:g.68669989C>T GRCh38
NC_000004.11:g.69535707C>T , CM000666.1:g.69535707C>T GRCh37
NC_000004.10:g.69218302C>T NCBI36
NG_052676.1:g.5788G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.630G>A MANE Select ENSP00000341045.5:p.Glu210=
ENST00000338206.5:c.630G>A ENSP00000341045.5:p.Glu210=
ENST00000616841.4:c.630G>A ENSP00000482004.1:p.Glu210=
NM_001076.3:c.630G>A NP_001067.2:p.Glu210=
NM_001076.4:c.630G>A MANE Select NP_001067.2:p.Glu210=
Search 100 bp 5'
Search 100 bp 3'