Canonical Allele Identifier: CA1063765170
Gene: UGT2B17 HGNC NCBI
UGT2B15 HGNC NCBI

Linked Data

dbSNP Id: rs6857249
gnomAD v3: 4-68569184-G-T
gnomAD v4: 4-68569184-G-T

Genomic Alleles

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

Transcript Alleles

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