Canonical Allele Identifier: CA1465794569
Gene: UGT2B15 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68670437G= , CM000666.2:g.68670437G= GRCh38
NC_000004.11:g.69536155G= , CM000666.1:g.69536155G= GRCh37
NC_000004.10:g.69218750G= NCBI36
NG_052676.1:g.5340C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.182C= MANE Select ENSP00000341045.5:p.Ser61=
ENST00000338206.5:c.182C= ENSP00000341045.5:p.Ser61=
ENST00000616841.4:c.182C= ENSP00000482004.1:p.Ser61=
NM_001076.3:c.182C= NP_001067.2:p.Ser61=
NM_001076.4:c.182C= MANE Select NP_001067.2:p.Ser61=
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