Canonical Allele Identifier: CA439835622

Gene: UGT2B17 UGT2B15

Linked Data

• MyVariant Identifiers: chr4:g.69432980C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.68567262C>G , CM000666.2:g.68567262C>G	GRCh38
NC_000004.11:g.69432980C>G , CM000666.1:g.69432980C>G	GRCh37
NC_000004.10:g.69115575C>G	NCBI36
NG_017033.1:g.6266G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000317746.3:c.724+499G>C (UGT2B17) MANE Select	ENSP00000320401.2:n.724+499G>C
ENST00000684088.1:c.-26-1542G>C (UGT2B17)	ENSP00000507374.1:n.-26-1542G>C
ENST00000317746.2:c.724+499G>C (UGT2B17)	ENSP00000320401.2:n.724+499G>C
ENST00000616841.4:c.1733-29736G>C (UGT2B15)	ENSP00000482004.1:n.1733-29736G>C
NM_001077.3:c.724+499G>C (UGT2B17)	NP_001068.1:n.724+499G>C
XM_024454205.1:c.724+499G>C (UGT2B17)	XP_024309973.1:n.724+499G>C
NM_001077.4:c.724+499G>C (UGT2B17) MANE Select	NP_001068.1:n.724+499G>C