Canonical Allele Identifier: CA1465820826
Gene: UGT2B15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68646812C= , CM000666.2:g.68646812C= GRCh38
NC_000004.11:g.69512530C= , CM000666.1:g.69512530C= GRCh37
NC_000004.10:g.69195125C= NCBI36
NG_052676.1:g.28965G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.*292G= MANE Select ENSP00000341045.5:n.*292G=
ENST00000338206.5:c.*292G= ENSP00000341045.5:n.*292G=
ENST00000616841.4:c.1732+153G= ENSP00000482004.1:n.1732+153G=
NM_001076.3:c.*292G= NP_001067.2:n.*292G=
NM_001076.4:c.*292G= MANE Select NP_001067.2:n.*292G=