Canonical Allele Identifier: CA357084953
Gene: UGT2B15 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.69535665C>G (hg19) chr4:g.68669947C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68669947C>G , CM000666.2:g.68669947C>G GRCh38
NC_000004.11:g.69535665C>G , CM000666.1:g.69535665C>G GRCh37
NC_000004.10:g.69218260C>G NCBI36
NG_052676.1:g.5830G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.672G>C MANE Select ENSP00000341045.5:p.Trp224Cys
ENST00000338206.5:c.672G>C ENSP00000341045.5:p.Trp224Cys
ENST00000616841.4:c.672G>C ENSP00000482004.1:p.Trp224Cys
NM_001076.3:c.672G>C NP_001067.2:p.Trp224Cys
NM_001076.4:c.672G>C MANE Select NP_001067.2:p.Trp224Cys
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