Canonical Allele Identifier: CA1465794973
Gene: UGT2B15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68670643T= , CM000666.2:g.68670643T= GRCh38
NC_000004.11:g.69536361T= , CM000666.1:g.69536361T= GRCh37
NC_000004.10:g.69218956T= NCBI36
NG_052676.1:g.5134A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.-25A= MANE Select ENSP00000341045.5:n.-25A=
NM_001076.3:c.-25A= NP_001067.2:n.-25A=
NM_001076.4:c.-25A= MANE Select NP_001067.2:n.-25A=