Canonical Allele Identifier: CA357087347
Gene: UGT2B15 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.69536205T>A (hg19) chr4:g.68670487T>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68670487T>A , CM000666.2:g.68670487T>A GRCh38
NC_000004.11:g.69536205T>A , CM000666.1:g.69536205T>A GRCh37
NC_000004.10:g.69218800T>A NCBI36
NG_052676.1:g.5290A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.132A>T MANE Select ENSP00000341045.5:p.Glu44Asp
ENST00000338206.5:c.132A>T ENSP00000341045.5:p.Glu44Asp
ENST00000616841.4:c.132A>T ENSP00000482004.1:p.Glu44Asp
NM_001076.3:c.132A>T NP_001067.2:p.Glu44Asp
NM_001076.4:c.132A>T MANE Select NP_001067.2:p.Glu44Asp
Search 100 bp 5'
Search 100 bp 3'