Canonical Allele Identifier: CA439934911
Gene: UGT2B15 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.69536172C>T (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68670454C>T , CM000666.2:g.68670454C>T GRCh38
NC_000004.11:g.69536172C>T , CM000666.1:g.69536172C>T GRCh37
NC_000004.10:g.69218767C>T NCBI36
NG_052676.1:g.5323G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.165G>A MANE Select ENSP00000341045.5:p.Val55=
ENST00000338206.5:c.165G>A ENSP00000341045.5:p.Val55=
ENST00000616841.4:c.165G>A ENSP00000482004.1:p.Val55=
NM_001076.3:c.165G>A NP_001067.2:p.Val55=
NM_001076.4:c.165G>A MANE Select NP_001067.2:p.Val55=
Search 100 bp 5'
Search 100 bp 3'