Canonical Allele Identifier: CA439705686
Gene: UGT2B15 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.69535668A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68669950A>G , CM000666.2:g.68669950A>G GRCh38
NC_000004.11:g.69535668A>G , CM000666.1:g.69535668A>G GRCh37
NC_000004.10:g.69218263A>G NCBI36
NG_052676.1:g.5827T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.669T>C MANE Select ENSP00000341045.5:p.Phe223=
ENST00000338206.5:c.669T>C ENSP00000341045.5:p.Phe223=
ENST00000616841.4:c.669T>C ENSP00000482004.1:p.Phe223=
NM_001076.3:c.669T>C NP_001067.2:p.Phe223=
NM_001076.4:c.669T>C MANE Select NP_001067.2:p.Phe223=
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