Canonical Allele Identifier: CA357083012
Gene: UGT2B15 HGNC NCBI

Linked Data

dbSNP Id: rs2109815543
MyVariant Identifiers: chr4:g.69512879A>C (hg19) chr4:g.68647161A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68647161A>C , CM000666.2:g.68647161A>C GRCh38
NC_000004.11:g.69512879A>C , CM000666.1:g.69512879A>C GRCh37
NC_000004.10:g.69195474A>C NCBI36
NG_052676.1:g.28616T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.1536T>G MANE Select ENSP00000341045.5:p.Phe512Leu
ENST00000338206.5:c.1536T>G ENSP00000341045.5:p.Phe512Leu
ENST00000616841.4:c.1536T>G ENSP00000482004.1:p.Phe512Leu
NM_001076.3:c.1536T>G NP_001067.2:p.Phe512Leu
NM_001076.4:c.1536T>G MANE Select NP_001067.2:p.Phe512Leu
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