Canonical Allele Identifier: CA2942659
Gene: UGT2B15 HGNC NCBI

Linked Data

dbSNP Id: rs201717195
ExAC: 4:69535654 T / C
gnomAD v2: 4-69535654-T-C
gnomAD v3: 4-68669936-T-C
gnomAD v4: 4-68669936-T-C
MyVariant Identifiers: chr4:g.69535654T>C (hg19) chr4:g.69535654_69535656delinsCAA (hg19) chr4:g.68669936T>C (hg38) chr4:g.68669936_68669938delinsCAA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68669936T>C , CM000666.2:g.68669936T>C GRCh38
NC_000004.11:g.69535654T>C , CM000666.1:g.69535654T>C GRCh37
NC_000004.10:g.69218249T>C NCBI36
NG_052676.1:g.5841A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.683A>G MANE Select ENSP00000341045.5:p.Tyr228Cys
ENST00000338206.5:c.683A>G ENSP00000341045.5:p.Tyr228Cys
ENST00000616841.4:c.683A>G ENSP00000482004.1:p.Tyr228Cys
NM_001076.3:c.683A>G NP_001067.2:p.Tyr228Cys
NM_001076.4:c.683A>G MANE Select NP_001067.2:p.Tyr228Cys
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