Canonical Allele Identifier: CA99379594
Gene: UGT2B17 HGNC NCBI
UGT2B15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68569184G>A , CM000666.2:g.68569184G>A GRCh38
NC_000004.11:g.69434902G>A , CM000666.1:g.69434902G>A GRCh37
NC_000004.10:g.69117497G>A NCBI36
NG_017033.1:g.4344C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000317746.3:c.-64-636C>T (UGT2B17) MANE Select ENSP00000320401.2:n.-64-636C>T
ENST00000684088.1:c.-26-3464C>T (UGT2B17) ENSP00000507374.1:n.-26-3464C>T
ENST00000616841.4:c.1733-31658C>T (UGT2B15) ENSP00000482004.1:n.1733-31658C>T
XM_024454205.1:c.-64-636C>T (UGT2B17) XP_024309973.1:n.-64-636C>T
NM_001077.4:c.-64-636C>T (UGT2B17) MANE Select NP_001068.1:n.-64-636C>T