Canonical Allele Identifier: CA2578102219
Gene: UGT2B15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68647054A>T , CM000666.2:g.68647054A>T GRCh38
NC_000004.11:g.69512772A>T , CM000666.1:g.69512772A>T GRCh37
NC_000004.10:g.69195367A>T NCBI36
NG_052676.1:g.28723T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.*50T>A MANE Select ENSP00000341045.5:n.*50T>A
ENST00000338206.5:c.*50T>A ENSP00000341045.5:n.*50T>A
ENST00000616841.4:c.1643T>A ENSP00000482004.1:n.1643T>A
NM_001076.3:c.*50T>A NP_001067.2:n.*50T>A
NM_001076.4:c.*50T>A MANE Select NP_001067.2:n.*50T>A