Canonical Allele Identifier: CA1465820690
Gene: UGT2B15 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68646623C= , CM000666.2:g.68646623C= GRCh38
NC_000004.11:g.69512341C= , CM000666.1:g.69512341C= GRCh37
NC_000004.10:g.69194936C= NCBI36
NG_052676.1:g.29154G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.*481G= MANE Select ENSP00000341045.5:n.*481G=
ENST00000616841.4:c.1732+342G= ENSP00000482004.1:n.1732+342G=
NM_001076.3:c.*481G= NP_001067.2:n.*481G=
NM_001076.4:c.*481G= MANE Select NP_001067.2:n.*481G=
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