Canonical Allele Identifier: CA357087134
Gene: UGT2B15 HGNC NCBI

Linked Data

gnomAD v4: 4-68670447-A-T
MyVariant Identifiers: chr4:g.69536165A>T (hg19) chr4:g.68670447A>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68670447A>T , CM000666.2:g.68670447A>T GRCh38
NC_000004.11:g.69536165A>T , CM000666.1:g.69536165A>T GRCh37
NC_000004.10:g.69218760A>T NCBI36
NG_052676.1:g.5330T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.172T>A MANE Select ENSP00000341045.5:p.Ser58Thr
ENST00000338206.5:c.172T>A ENSP00000341045.5:p.Ser58Thr
ENST00000616841.4:c.172T>A ENSP00000482004.1:p.Ser58Thr
NM_001076.3:c.172T>A NP_001067.2:p.Ser58Thr
NM_001076.4:c.172T>A MANE Select NP_001067.2:p.Ser58Thr
Search 100 bp 5'
Search 100 bp 3'