Canonical Allele Identifier: CA797765386

Gene: UGT2B17 UGT2B15

Linked Data

• dbSNP Id: rs1300910946
• gnomAD v3: 4-68567276-C-A
• gnomAD v4: 4-68567276-C-A
• MyVariant Identifiers: chr4:g.69432994C>A (hg19) ; chr4:g.68567276C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.68567276C>A , CM000666.2:g.68567276C>A	GRCh38
NC_000004.11:g.69432994C>A , CM000666.1:g.69432994C>A	GRCh37
NC_000004.10:g.69115589C>A	NCBI36
NG_017033.1:g.6252G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000317746.3:c.724+485G>T (UGT2B17) MANE Select	ENSP00000320401.2:n.724+485G>T
ENST00000684088.1:c.-26-1556G>T (UGT2B17)	ENSP00000507374.1:n.-26-1556G>T
ENST00000317746.2:c.724+485G>T (UGT2B17)	ENSP00000320401.2:n.724+485G>T
ENST00000616841.4:c.1733-29750G>T (UGT2B15)	ENSP00000482004.1:n.1733-29750G>T
NM_001077.3:c.724+485G>T (UGT2B17)	NP_001068.1:n.724+485G>T
XM_024454205.1:c.724+485G>T (UGT2B17)	XP_024309973.1:n.724+485G>T
NM_001077.4:c.724+485G>T (UGT2B17) MANE Select	NP_001068.1:n.724+485G>T