Canonical Allele Identifier: CA1465794188
Gene: UGT2B15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68670207T= , CM000666.2:g.68670207T= GRCh38
NC_000004.11:g.69535925T= , CM000666.1:g.69535925T= GRCh37
NC_000004.10:g.69218520T= NCBI36
NG_052676.1:g.5570A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.412A= MANE Select ENSP00000341045.5:p.Met138=
ENST00000338206.5:c.412A= ENSP00000341045.5:p.Met138=
ENST00000616841.4:c.412A= ENSP00000482004.1:p.Met138=
NM_001076.3:c.412A= NP_001067.2:p.Met138=
NM_001076.4:c.412A= MANE Select NP_001067.2:p.Met138=