Canonical Allele Identifier: CA439935368
Gene: UGT2B15 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.69535992T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68670274T>C , CM000666.2:g.68670274T>C GRCh38
NC_000004.11:g.69535992T>C , CM000666.1:g.69535992T>C GRCh37
NC_000004.10:g.69218587T>C NCBI36
NG_052676.1:g.5503A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000338206.6:c.345A>G MANE Select ENSP00000341045.5:p.Glu115=
ENST00000338206.5:c.345A>G ENSP00000341045.5:p.Glu115=
ENST00000616841.4:c.345A>G ENSP00000482004.1:p.Glu115=
NM_001076.3:c.345A>G NP_001067.2:p.Glu115=
NM_001076.4:c.345A>G MANE Select NP_001067.2:p.Glu115=