Canonical Allele Identifier: CA439705636
Gene: UGT2B15 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.69535623A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68669905A>G , CM000666.2:g.68669905A>G GRCh38
NC_000004.11:g.69535623A>G , CM000666.1:g.69535623A>G GRCh37
NC_000004.10:g.69218218A>G NCBI36
NG_052676.1:g.5872T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.714T>C MANE Select ENSP00000341045.5:p.Ser238=
ENST00000338206.5:c.714T>C ENSP00000341045.5:p.Ser238=
ENST00000616841.4:c.714T>C ENSP00000482004.1:p.Ser238=
NM_001076.3:c.714T>C NP_001067.2:p.Ser238=
NM_001076.4:c.714T>C MANE Select NP_001067.2:p.Ser238=
Search 100 bp 5'
Search 100 bp 3'