Canonical Allele Identifier: CA552412098

Gene: UGT2B17 UGT2B15

Linked Data

• dbSNP Id: rs1295939950
• gnomAD v2: 4-69425370-A-G
• gnomAD v3: 4-68559652-A-G
• gnomAD v4: 4-68559652-A-G
• MyVariant Identifiers: chr4:g.69425370A>G (hg19) ; chr4:g.68559652A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.68559652A>G , CM000666.2:g.68559652A>G	GRCh38
NC_000004.11:g.69425370A>G , CM000666.1:g.69425370A>G	GRCh37
NC_000004.10:g.69107965A>G	NCBI36
NG_017033.1:g.13876T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000317746.3:c.1005+885T>C (UGT2B17) MANE Select	ENSP00000320401.2:n.1005+885T>C
ENST00000684088.1:c.255+885T>C (UGT2B17)	ENSP00000507374.1:n.255+885T>C
ENST00000317746.2:c.1005+885T>C (UGT2B17)	ENSP00000320401.2:n.1005+885T>C
ENST00000616841.4:c.1733-22126T>C (UGT2B15)	ENSP00000482004.1:n.1733-22126T>C
NM_001077.3:c.1005+885T>C (UGT2B17)	NP_001068.1:n.1005+885T>C
XM_024454205.1:c.1005+885T>C (UGT2B17)	XP_024309973.1:n.1005+885T>C
NM_001077.4:c.1005+885T>C (UGT2B17) MANE Select	NP_001068.1:n.1005+885T>C