Canonical Allele Identifier: CA1465794466
Gene: UGT2B15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68670372T= , CM000666.2:g.68670372T= GRCh38
NC_000004.11:g.69536090T= , CM000666.1:g.69536090T= GRCh37
NC_000004.10:g.69218685T= NCBI36
NG_052676.1:g.5405A=

Transcript Alleles

HGVS Amino-acid change
ENST00000338206.6:c.247A= MANE Select ENSP00000341045.5:p.Lys83=
ENST00000338206.5:c.247A= ENSP00000341045.5:p.Lys83=
ENST00000616841.4:c.247A= ENSP00000482004.1:p.Lys83=
NM_001076.3:c.247A= NP_001067.2:p.Lys83=
NM_001076.4:c.247A= MANE Select NP_001067.2:p.Lys83=