Canonical Allele Identifier: CA1465820752
Gene: UGT2B15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68646724G= , CM000666.2:g.68646724G= GRCh38
NC_000004.11:g.69512442G= , CM000666.1:g.69512442G= GRCh37
NC_000004.10:g.69195037G= NCBI36
NG_052676.1:g.29053C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.*380C= MANE Select ENSP00000341045.5:n.*380C=
ENST00000338206.5:c.*380C= ENSP00000341045.5:n.*380C=
ENST00000616841.4:c.1732+241C= ENSP00000482004.1:n.1732+241C=
NM_001076.3:c.*380C= NP_001067.2:n.*380C=
NM_001076.4:c.*380C= MANE Select NP_001067.2:n.*380C=