Canonical Allele Identifier: CA797765523

Gene: UGT2B17 UGT2B15

Linked Data

• dbSNP Id: rs1307813160
• gnomAD v3: 4-68567509-A-C
• gnomAD v4: 4-68567509-A-C
• MyVariant Identifiers: chr4:g.69433227A>C (hg19) ; chr4:g.68567509A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.68567509A>C , CM000666.2:g.68567509A>C	GRCh38
NC_000004.11:g.69433227A>C , CM000666.1:g.69433227A>C	GRCh37
NC_000004.10:g.69115822A>C	NCBI36
NG_017033.1:g.6019T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317746.3:c.724+252T>G (UGT2B17) MANE Select	ENSP00000320401.2:n.724+252T>G
ENST00000684088.1:c.-26-1789T>G (UGT2B17)	ENSP00000507374.1:n.-26-1789T>G
ENST00000317746.2:c.724+252T>G (UGT2B17)	ENSP00000320401.2:n.724+252T>G
ENST00000616841.4:c.1733-29983T>G (UGT2B15)	ENSP00000482004.1:n.1733-29983T>G
NM_001077.3:c.724+252T>G (UGT2B17)	NP_001068.1:n.724+252T>G
XM_024454205.1:c.724+252T>G (UGT2B17)	XP_024309973.1:n.724+252T>G
NM_001077.4:c.724+252T>G (UGT2B17) MANE Select	NP_001068.1:n.724+252T>G