Canonical Allele Identifier: CA439934945
Gene: UGT2B15 HGNC NCBI

Linked Data

dbSNP Id: rs1338845096
gnomAD v2: 4-69536202-C-T
gnomAD v4: 4-68670484-C-T
MyVariant Identifiers: chr4:g.69536202C>T (hg19) chr4:g.68670484C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68670484C>T , CM000666.2:g.68670484C>T GRCh38
NC_000004.11:g.69536202C>T , CM000666.1:g.69536202C>T GRCh37
NC_000004.10:g.69218797C>T NCBI36
NG_052676.1:g.5293G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.135G>A MANE Select ENSP00000341045.5:p.Glu45=
ENST00000338206.5:c.135G>A ENSP00000341045.5:p.Glu45=
ENST00000616841.4:c.135G>A ENSP00000482004.1:p.Glu45=
NM_001076.3:c.135G>A NP_001067.2:p.Glu45=
NM_001076.4:c.135G>A MANE Select NP_001067.2:p.Glu45=
Search 100 bp 5'
Search 100 bp 3'