Canonical Allele Identifier: CA352739552

Gene: IMPDH2

Linked Data

• dbSNP Id: rs2093200579
• MyVariant Identifiers: chr3:g.49064014T>C (hg19) ; chr3:g.49026581T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49026581T>C , CM000665.2:g.49026581T>C	GRCh38
NC_000003.11:g.49064014T>C , CM000665.1:g.49064014T>C	GRCh37
NC_000003.10:g.49039018T>C	NCBI36
NG_012091.1:g.7862A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000703936.1:c.2888A>G	ENSP00000515567.1:p.Gln963Arg
ENST00000703937.1:c.*1949A>G	ENSP00000515568.1:n.*1949A>G
ENST00000326739.9:c.848A>G MANE Select	ENSP00000321584.4:p.Gln283Arg
ENST00000429182.6:c.848A>G	ENSP00000393525.2:p.Gln283Arg
ENST00000442157.2:c.773A>G	ENSP00000403502.2:p.Gln258Arg
ENST00000462980.2:n.1363A>G
ENST00000472328.2:n.914A>G
ENST00000491610.2:n.808A>G
ENST00000676607.1:n.1144A>G
ENST00000676627.1:n.1578A>G
ENST00000676708.1:n.2128A>G
ENST00000676864.1:n.1997A>G
ENST00000677010.1:c.872A>G	ENSP00000503089.1:p.Gln291Arg
ENST00000677108.1:n.2831A>G
ENST00000677168.1:n.1320A>G
ENST00000677185.1:n.1411A>G
ENST00000677205.1:n.1632A>G
ENST00000677344.1:n.2122A>G
ENST00000677480.1:c.*525A>G	ENSP00000504378.1:n.*525A>G
ENST00000677519.1:n.1558A>G
ENST00000677593.1:n.1404A>G
ENST00000677740.1:n.2353A>G
ENST00000677991.1:n.2021A>G
ENST00000678001.1:n.1341A>G
ENST00000678085.1:n.1481A>G
ENST00000678177.1:n.2774A>G
ENST00000678603.1:n.1926A>G
ENST00000678724.1:c.773A>G	ENSP00000503874.1:p.Gln258Arg
ENST00000678920.1:n.1006A>G
ENST00000679019.1:n.1695A>G
ENST00000679117.1:c.*663A>G	ENSP00000503240.1:n.*663A>G
ENST00000679339.1:n.1689A>G
ENST00000326739.8:c.848A>G	ENSP00000321584.4:p.Gln283Arg
ENST00000429182.5:c.642A>G
ENST00000442157.1:c.773A>G	ENSP00000403502.1:p.Gln258Arg
ENST00000462980.1:n.750A>G
ENST00000491610.1:n.808A>G
NM_000884.2:c.848A>G	NP_000875.2:p.Gln283Arg
XM_006713128.2:c.1058A>G	XP_006713191.1:p.Gln353Arg
XM_006713128.3:c.1058A>G	XP_006713191.1:p.Gln353Arg
XM_017006349.1:c.983A>G	XP_016861838.1:p.Gln328Arg
XM_017006350.1:c.983A>G	XP_016861839.1:p.Gln328Arg
NM_000884.3:c.848A>G MANE Select	NP_000875.2:p.Gln283Arg