Canonical Allele Identifier: CA439705645
Gene: UGT2B15 HGNC NCBI

Linked Data

dbSNP Id: rs1560612890
MyVariant Identifiers: chr4:g.69535632C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68669914C>T , CM000666.2:g.68669914C>T GRCh38
NC_000004.11:g.69535632C>T , CM000666.1:g.69535632C>T GRCh37
NC_000004.10:g.69218227C>T NCBI36
NG_052676.1:g.5863G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.705G>A MANE Select ENSP00000341045.5:p.Gln235=
ENST00000338206.5:c.705G>A ENSP00000341045.5:p.Gln235=
ENST00000616841.4:c.705G>A ENSP00000482004.1:p.Gln235=
NM_001076.3:c.705G>A NP_001067.2:p.Gln235=
NM_001076.4:c.705G>A MANE Select NP_001067.2:p.Gln235=
Search 100 bp 5'
Search 100 bp 3'