Canonical Allele Identifier: CA797760183
Gene: UGT2B17 HGNC NCBI
UGT2B15 HGNC NCBI

Linked Data

dbSNP Id: rs1163260471
MyVariant Identifiers: chr4:g.69425590A>T (hg19) chr4:g.68559872A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.68559872A>T , CM000666.2:g.68559872A>T GRCh38
NC_000004.11:g.69425590A>T , CM000666.1:g.69425590A>T GRCh37
NC_000004.10:g.69108185A>T NCBI36
NG_017033.1:g.13656T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000317746.3:c.1005+665T>A (UGT2B17) MANE Select ENSP00000320401.2:n.1005+665T>A
ENST00000684088.1:c.255+665T>A (UGT2B17) ENSP00000507374.1:n.255+665T>A
ENST00000317746.2:c.1005+665T>A (UGT2B17) ENSP00000320401.2:n.1005+665T>A
ENST00000616841.4:c.1733-22346T>A (UGT2B15) ENSP00000482004.1:n.1733-22346T>A
NM_001077.3:c.1005+665T>A (UGT2B17) NP_001068.1:n.1005+665T>A
XM_024454205.1:c.1005+665T>A (UGT2B17) XP_024309973.1:n.1005+665T>A
NM_001077.4:c.1005+665T>A (UGT2B17) MANE Select NP_001068.1:n.1005+665T>A
Search 100 bp 5'
Search 100 bp 3'