Canonical Allele Identifier: CA357085102
Gene: UGT2B15 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68670008T>C , CM000666.2:g.68670008T>C GRCh38
NC_000004.11:g.69535726T>C , CM000666.1:g.69535726T>C GRCh37
NC_000004.10:g.69218321T>C NCBI36
NG_052676.1:g.5769A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.611A>G MANE Select ENSP00000341045.5:p.Asp204Gly
ENST00000338206.5:c.611A>G ENSP00000341045.5:p.Asp204Gly
ENST00000616841.4:c.611A>G ENSP00000482004.1:p.Asp204Gly
NM_001076.3:c.611A>G NP_001067.2:p.Asp204Gly
NM_001076.4:c.611A>G MANE Select NP_001067.2:p.Asp204Gly