Canonical Allele Identifier: CA439934683
Gene: UGT2B15 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.69512864G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68647146G>A , CM000666.2:g.68647146G>A GRCh38
NC_000004.11:g.69512864G>A , CM000666.1:g.69512864G>A GRCh37
NC_000004.10:g.69195459G>A NCBI36
NG_052676.1:g.28631C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.1551C>T MANE Select ENSP00000341045.5:p.Phe517=
ENST00000338206.5:c.1551C>T ENSP00000341045.5:p.Phe517=
ENST00000616841.4:c.1551C>T ENSP00000482004.1:p.Phe517=
NM_001076.3:c.1551C>T NP_001067.2:p.Phe517=
NM_001076.4:c.1551C>T MANE Select NP_001067.2:p.Phe517=
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Search 100 bp 3'