Canonical Allele Identifier: CA439705772
Gene: UGT2B15 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.69535761A>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68670043A>C , CM000666.2:g.68670043A>C GRCh38
NC_000004.11:g.69535761A>C , CM000666.1:g.69535761A>C GRCh37
NC_000004.10:g.69218356A>C NCBI36
NG_052676.1:g.5734T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.576T>G MANE Select ENSP00000341045.5:p.Pro192=
ENST00000338206.5:c.576T>G ENSP00000341045.5:p.Pro192=
ENST00000616841.4:c.576T>G ENSP00000482004.1:p.Pro192=
NM_001076.3:c.576T>G NP_001067.2:p.Pro192=
NM_001076.4:c.576T>G MANE Select NP_001067.2:p.Pro192=
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