Canonical Allele Identifier: CA439935193
Gene: UGT2B15 HGNC NCBI

Linked Data

dbSNP Id: rs1733260400
MyVariant Identifiers: chr4:g.69535839G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68670121G>A , CM000666.2:g.68670121G>A GRCh38
NC_000004.11:g.69535839G>A , CM000666.1:g.69535839G>A GRCh37
NC_000004.10:g.69218434G>A NCBI36
NG_052676.1:g.5656C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.498C>T MANE Select ENSP00000341045.5:p.Asn166=
ENST00000338206.5:c.498C>T ENSP00000341045.5:p.Asn166=
ENST00000616841.4:c.498C>T ENSP00000482004.1:p.Asn166=
NM_001076.3:c.498C>T NP_001067.2:p.Asn166=
NM_001076.4:c.498C>T MANE Select NP_001067.2:p.Asn166=
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Search 100 bp 3'