Canonical Allele Identifier: CA357083014
Gene: UGT2B15 HGNC NCBI

Linked Data

dbSNP Id: rs1270580253
gnomAD v2: 4-69512880-A-C
gnomAD v3: 4-68647162-A-C
gnomAD v4: 4-68647162-A-C
MyVariant Identifiers: chr4:g.69512880A>C (hg19) chr4:g.68647162A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68647162A>C , CM000666.2:g.68647162A>C GRCh38
NC_000004.11:g.69512880A>C , CM000666.1:g.69512880A>C GRCh37
NC_000004.10:g.69195475A>C NCBI36
NG_052676.1:g.28615T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.1535T>G MANE Select ENSP00000341045.5:p.Phe512Cys
ENST00000338206.5:c.1535T>G ENSP00000341045.5:p.Phe512Cys
ENST00000616841.4:c.1535T>G ENSP00000482004.1:p.Phe512Cys
NM_001076.3:c.1535T>G NP_001067.2:p.Phe512Cys
NM_001076.4:c.1535T>G MANE Select NP_001067.2:p.Phe512Cys
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