Canonical Allele Identifier: CA2942353
Gene: UGT2B15 HGNC NCBI

Linked Data

dbSNP Id: rs765074066
ExAC: 4:69512831 T / C
gnomAD v2: 4-69512831-T-C
gnomAD v4: 4-68647113-T-C
MyVariant Identifiers: chr4:g.69512831T>C (hg19) chr4:g.69512831_69512834delinsCTTC (hg19) chr4:g.68647113T>C (hg38) chr4:g.68647113_68647116delinsCTTC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68647113T>C , CM000666.2:g.68647113T>C GRCh38
NC_000004.11:g.69512831T>C , CM000666.1:g.69512831T>C GRCh37
NC_000004.10:g.69195426T>C NCBI36
NG_052676.1:g.28664A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.1584A>G MANE Select ENSP00000341045.5:p.Lys528=
ENST00000338206.5:c.1584A>G ENSP00000341045.5:p.Lys528=
ENST00000616841.4:c.1584A>G ENSP00000482004.1:p.Lys528=
NM_001076.3:c.1584A>G NP_001067.2:p.Lys528=
NM_001076.4:c.1584A>G MANE Select NP_001067.2:p.Lys528=
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