Canonical Allele Identifier: CA1465794952
Gene: UGT2B15 HGNC NCBI

Linked Data

dbSNP Id: rs1733286614
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68670630G>A , CM000666.2:g.68670630G>A GRCh38
NC_000004.11:g.69536348G>A , CM000666.1:g.69536348G>A GRCh37
NC_000004.10:g.69218943G>A NCBI36
NG_052676.1:g.5147C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000338206.6:c.-12C>T MANE Select ENSP00000341045.5:n.-12C>T
NM_001076.3:c.-12C>T NP_001067.2:n.-12C>T
NM_001076.4:c.-12C>T MANE Select NP_001067.2:n.-12C>T
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