Canonical Allele Identifier: CA439705828
Gene: UGT2B15 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.69536331A>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68670613A>C , CM000666.2:g.68670613A>C GRCh38
NC_000004.11:g.69536331A>C , CM000666.1:g.69536331A>C GRCh37
NC_000004.10:g.69218926A>C NCBI36
NG_052676.1:g.5164T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.6T>G MANE Select ENSP00000341045.5:p.Ser2=
ENST00000338206.5:c.6T>G ENSP00000341045.5:p.Ser2=
ENST00000616841.4:c.6T>G ENSP00000482004.1:p.Ser2=
NM_001076.3:c.6T>G NP_001067.2:p.Ser2=
NM_001076.4:c.6T>G MANE Select NP_001067.2:p.Ser2=
Search 100 bp 5'
Search 100 bp 3'