Canonical Allele Identifier: CA439934679
Gene: UGT2B15 HGNC NCBI

Linked Data

dbSNP Id: rs1456391097
gnomAD v2: 4-69512861-T-A
MyVariant Identifiers: chr4:g.69512861T>A (hg19) chr4:g.68647143T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68647143T>A , CM000666.2:g.68647143T>A GRCh38
NC_000004.11:g.69512861T>A , CM000666.1:g.69512861T>A GRCh37
NC_000004.10:g.69195456T>A NCBI36
NG_052676.1:g.28634A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.1554A>T MANE Select ENSP00000341045.5:p.Arg518=
ENST00000338206.5:c.1554A>T ENSP00000341045.5:p.Arg518=
ENST00000616841.4:c.1554A>T ENSP00000482004.1:p.Arg518=
NM_001076.3:c.1554A>T NP_001067.2:p.Arg518=
NM_001076.4:c.1554A>T MANE Select NP_001067.2:p.Arg518=
Search 100 bp 5'
Search 100 bp 3'