Canonical Allele Identifier: CA1465760664
Gene: UGT2B17 HGNC NCBI
UGT2B15 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68559681C= , CM000666.2:g.68559681C= GRCh38
NC_000004.11:g.69425399C= , CM000666.1:g.69425399C= GRCh37
NC_000004.10:g.69107994C= NCBI36
NG_017033.1:g.13847G=

Transcript Alleles

HGVS Amino-acid change
ENST00000317746.3:c.1005+856G= (UGT2B17) MANE Select ENSP00000320401.2:n.1005+856G=
ENST00000684088.1:c.255+856G= (UGT2B17) ENSP00000507374.1:n.255+856G=
ENST00000317746.2:c.1005+856G= (UGT2B17) ENSP00000320401.2:n.1005+856G=
ENST00000616841.4:c.1733-22155G= (UGT2B15) ENSP00000482004.1:n.1733-22155G=
NM_001077.3:c.1005+856G= (UGT2B17) NP_001068.1:n.1005+856G=
XM_024454205.1:c.1005+856G= (UGT2B17) XP_024309973.1:n.1005+856G=
NM_001077.4:c.1005+856G= (UGT2B17) MANE Select NP_001068.1:n.1005+856G=
Search 100 bp 5'
Search 100 bp 3'