Canonical Allele Identifier: CA357087902
Gene: UGT2B15 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.69536296A>T (hg19) chr4:g.68670578A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68670578A>T , CM000666.2:g.68670578A>T GRCh38
NC_000004.11:g.69536296A>T , CM000666.1:g.69536296A>T GRCh37
NC_000004.10:g.69218891A>T NCBI36
NG_052676.1:g.5199T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.41T>A MANE Select ENSP00000341045.5:p.Leu14His
ENST00000338206.5:c.41T>A ENSP00000341045.5:p.Leu14His
ENST00000616841.4:c.41T>A ENSP00000482004.1:p.Leu14His
NM_001076.3:c.41T>A NP_001067.2:p.Leu14His
NM_001076.4:c.41T>A MANE Select NP_001067.2:p.Leu14His
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