Canonical Allele Identifier: CA1465821000
Gene: UGT2B15 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68647120T= , CM000666.2:g.68647120T= GRCh38
NC_000004.11:g.69512838T= , CM000666.1:g.69512838T= GRCh37
NC_000004.10:g.69195433T= NCBI36
NG_052676.1:g.28657A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.1577A= MANE Select ENSP00000341045.5:p.Lys526=
ENST00000338206.5:c.1577A= ENSP00000341045.5:p.Lys526=
ENST00000616841.4:c.1577A= ENSP00000482004.1:p.Lys526=
NM_001076.3:c.1577A= NP_001067.2:p.Lys526=
NM_001076.4:c.1577A= MANE Select NP_001067.2:p.Lys526=
Search 100 bp 5'
Search 100 bp 3'