Canonical Allele Identifier: CA439700481
Gene: UGT2B15 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.69512397A>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68646679A>C , CM000666.2:g.68646679A>C GRCh38
NC_000004.11:g.69512397A>C , CM000666.1:g.69512397A>C GRCh37
NC_000004.10:g.69194992A>C NCBI36
NG_052676.1:g.29098T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.*425T>G MANE Select ENSP00000341045.5:n.*425T>G
ENST00000338206.5:c.*425T>G ENSP00000341045.5:n.*425T>G
ENST00000616841.4:c.1732+286T>G ENSP00000482004.1:n.1732+286T>G
NM_001076.3:c.*425T>G NP_001067.2:n.*425T>G
NM_001076.4:c.*425T>G MANE Select NP_001067.2:n.*425T>G
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