Canonical Allele Identifier: CA2942348
Gene: UGT2B15 HGNC NCBI

Linked Data

dbSNP Id: rs760216669
ExAC: 4:69512825 A / T
gnomAD v2: 4-69512825-A-T
gnomAD v4: 4-68647107-A-T
MyVariant Identifiers: chr4:g.69512825A>T (hg19) chr4:g.68647107A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68647107A>T , CM000666.2:g.68647107A>T GRCh38
NC_000004.11:g.69512825A>T , CM000666.1:g.69512825A>T GRCh37
NC_000004.10:g.69195420A>T NCBI36
NG_052676.1:g.28670T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.1590T>A MANE Select ENSP00000341045.5:p.Asp530Glu
ENST00000338206.5:c.1590T>A ENSP00000341045.5:p.Asp530Glu
ENST00000616841.4:c.1590T>A ENSP00000482004.1:p.Asp530Glu
NM_001076.3:c.1590T>A NP_001067.2:p.Asp530Glu
NM_001076.4:c.1590T>A MANE Select NP_001067.2:p.Asp530Glu
Search 100 bp 5'
Search 100 bp 3'