Canonical Allele Identifier: CA357087079
Gene: UGT2B15 HGNC NCBI

Linked Data

dbSNP Id: rs1733277211

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68670437G>A , CM000666.2:g.68670437G>A GRCh38
NC_000004.11:g.69536155G>A , CM000666.1:g.69536155G>A GRCh37
NC_000004.10:g.69218750G>A NCBI36
NG_052676.1:g.5340C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.182C>T MANE Select ENSP00000341045.5:p.Ser61Phe
ENST00000338206.5:c.182C>T ENSP00000341045.5:p.Ser61Phe
ENST00000616841.4:c.182C>T ENSP00000482004.1:p.Ser61Phe
NM_001076.3:c.182C>T NP_001067.2:p.Ser61Phe
NM_001076.4:c.182C>T MANE Select NP_001067.2:p.Ser61Phe