Canonical Allele Identifier: CA1465794924
Gene: UGT2B15 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68670619C= , CM000666.2:g.68670619C= GRCh38
NC_000004.11:g.69536337C= , CM000666.1:g.69536337C= GRCh37
NC_000004.10:g.69218932C= NCBI36
NG_052676.1:g.5158G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.-1G= MANE Select ENSP00000341045.5:n.-1G=
ENST00000338206.5:c.-1G= ENSP00000341045.5:n.-1G=
NM_001076.3:c.-1G= NP_001067.2:n.-1G=
NM_001076.4:c.-1G= MANE Select NP_001067.2:n.-1G=
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