Canonical Allele Identifier: CA99379508
Gene: UGT2B17 HGNC NCBI
UGT2B15 HGNC NCBI

Linked Data

dbSNP Id: rs6552182

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68567230T>C , CM000666.2:g.68567230T>C GRCh38
NC_000004.11:g.69432948T>C , CM000666.1:g.69432948T>C GRCh37
NC_000004.10:g.69115543T>C NCBI36
NG_017033.1:g.6298A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000317746.3:c.724+531A>G (UGT2B17) MANE Select ENSP00000320401.2:n.724+531A>G
ENST00000684088.1:c.-26-1510A>G (UGT2B17) ENSP00000507374.1:n.-26-1510A>G
ENST00000317746.2:c.724+531A>G (UGT2B17) ENSP00000320401.2:n.724+531A>G
ENST00000616841.4:n.1733-29704A>G (UGT2B15) ENSP00000482004.1:n.1733-29704A>G
NM_001077.3:c.724+531A>G (UGT2B17) NP_001068.1:n.724+531A>G
XM_024454205.1:c.724+531A>G (UGT2B17) XP_024309973.1:n.724+531A>G
NM_001077.4:c.724+531A>G (UGT2B17) MANE Select NP_001068.1:n.724+531A>G