Canonical Allele Identifier: CA1465793671
Gene: UGT2B15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68669923C= , CM000666.2:g.68669923C= GRCh38
NC_000004.11:g.69535641C= , CM000666.1:g.69535641C= GRCh37
NC_000004.10:g.69218236C= NCBI36
NG_052676.1:g.5854G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.696G= MANE Select ENSP00000341045.5:p.Lys232=
ENST00000338206.5:c.696G= ENSP00000341045.5:p.Lys232=
ENST00000616841.4:c.696G= ENSP00000482004.1:p.Lys232=
NM_001076.3:c.696G= NP_001067.2:p.Lys232=
NM_001076.4:c.696G= MANE Select NP_001067.2:p.Lys232=