Canonical Allele Identifier: CA98760679
Gene: UGT2B15 HGNC NCBI

Linked Data

ClinVar Variation Id: 3186192
ClinVar RCV Id: RCV004479590
dbSNP Id: rs374449593
gnomAD v2: 4-69536294-T-C
gnomAD v3: 4-68670576-T-C
gnomAD v4: 4-68670576-T-C
MyVariant Identifiers: chr4:g.69536294T>C (hg19) chr4:g.68670576T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68670576T>C , CM000666.2:g.68670576T>C GRCh38
NC_000004.11:g.69536294T>C , CM000666.1:g.69536294T>C GRCh37
NC_000004.10:g.69218889T>C NCBI36
NG_052676.1:g.5201A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.43A>G MANE Select ENSP00000341045.5:p.Ser15Gly
ENST00000338206.5:c.43A>G ENSP00000341045.5:p.Ser15Gly
ENST00000616841.4:c.43A>G ENSP00000482004.1:p.Ser15Gly
NM_001076.3:c.43A>G NP_001067.2:p.Ser15Gly
NM_001076.4:c.43A>G MANE Select NP_001067.2:p.Ser15Gly
Search 100 bp 5'
Search 100 bp 3'