Canonical Allele Identifier: CA1465761151

Gene: UGT2B17 UGT2B15

Linked Data

• dbSNP Id: rs1731075730

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.68560088G>C , CM000666.2:g.68560088G>C	GRCh38
NC_000004.11:g.69425806G>C , CM000666.1:g.69425806G>C	GRCh37
NC_000004.10:g.69108401G>C	NCBI36
NG_017033.1:g.13440C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317746.3:c.1005+449C>G (UGT2B17) MANE Select	ENSP00000320401.2:n.1005+449C>G
ENST00000684088.1:c.255+449C>G (UGT2B17)	ENSP00000507374.1:n.255+449C>G
ENST00000317746.2:c.1005+449C>G (UGT2B17)	ENSP00000320401.2:n.1005+449C>G
ENST00000616841.4:c.1733-22562C>G (UGT2B15)	ENSP00000482004.1:n.1733-22562C>G
NM_001077.3:c.1005+449C>G (UGT2B17)	NP_001068.1:n.1005+449C>G
XM_024454205.1:c.1005+449C>G (UGT2B17)	XP_024309973.1:n.1005+449C>G
NM_001077.4:c.1005+449C>G (UGT2B17) MANE Select	NP_001068.1:n.1005+449C>G