Canonical Allele Identifier: CA357086959
Gene: UGT2B15 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.69536131G>T (hg19) chr4:g.68670413G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68670413G>T , CM000666.2:g.68670413G>T GRCh38
NC_000004.11:g.69536131G>T , CM000666.1:g.69536131G>T GRCh37
NC_000004.10:g.69218726G>T NCBI36
NG_052676.1:g.5364C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.206C>A MANE Select ENSP00000341045.5:p.Ser69Ter
ENST00000338206.5:c.206C>A ENSP00000341045.5:p.Ser69Ter
ENST00000616841.4:c.206C>A ENSP00000482004.1:p.Ser69Ter
NM_001076.3:c.206C>A NP_001067.2:p.Ser69Ter
NM_001076.4:c.206C>A MANE Select NP_001067.2:p.Ser69Ter
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