Canonical Allele Identifier: CA439934665
Gene: UGT2B15 HGNC NCBI

Linked Data

COSMIC: COSM734933
MyVariant Identifiers: chr4:g.69512834C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68647116C>T , CM000666.2:g.68647116C>T GRCh38
NC_000004.11:g.69512834C>T , CM000666.1:g.69512834C>T GRCh37
NC_000004.10:g.69195429C>T NCBI36
NG_052676.1:g.28661G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.1581G>A MANE Select ENSP00000341045.5:p.Lys527=
ENST00000338206.5:c.1581G>A ENSP00000341045.5:p.Lys527=
ENST00000616841.4:c.1581G>A ENSP00000482004.1:p.Lys527=
NM_001076.3:c.1581G>A NP_001067.2:p.Lys527=
NM_001076.4:c.1581G>A MANE Select NP_001067.2:p.Lys527=
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