Canonical Allele Identifier: CA1465760896
Gene: UGT2B17 HGNC NCBI
UGT2B15 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68559902A= , CM000666.2:g.68559902A= GRCh38
NC_000004.11:g.69425620A= , CM000666.1:g.69425620A= GRCh37
NC_000004.10:g.69108215A= NCBI36
NG_017033.1:g.13626T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000317746.3:c.1005+635T= (UGT2B17) MANE Select ENSP00000320401.2:n.1005+635T=
ENST00000684088.1:c.255+635T= (UGT2B17) ENSP00000507374.1:n.255+635T=
ENST00000317746.2:c.1005+635T= (UGT2B17) ENSP00000320401.2:n.1005+635T=
ENST00000616841.4:c.1733-22376T= (UGT2B15) ENSP00000482004.1:n.1733-22376T=
NM_001077.3:c.1005+635T= (UGT2B17) NP_001068.1:n.1005+635T=
XM_024454205.1:c.1005+635T= (UGT2B17) XP_024309973.1:n.1005+635T=
NM_001077.4:c.1005+635T= (UGT2B17) MANE Select NP_001068.1:n.1005+635T=
Search 100 bp 5'
Search 100 bp 3'