Canonical Allele Identifier: CA433629652

Gene: IMPDH2

Linked Data

• MyVariant Identifiers: chr3:g.49064269G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49026836G>T , CM000665.2:g.49026836G>T	GRCh38
NC_000003.11:g.49064269G>T , CM000665.1:g.49064269G>T	GRCh37
NC_000003.10:g.49039273G>T	NCBI36
NG_012091.1:g.7607C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703936.1:c.2710C>A	ENSP00000515567.1:p.Arg904=
ENST00000703937.1:c.*1771C>A	ENSP00000515568.1:n.*1771C>A
ENST00000326739.9:c.670C>A MANE Select	ENSP00000321584.4:p.Arg224=
ENST00000429182.6:c.670C>A	ENSP00000393525.2:p.Arg224=
ENST00000442157.2:c.595C>A	ENSP00000403502.2:p.Arg199=
ENST00000462980.2:n.1185C>A
ENST00000472328.2:n.736C>A
ENST00000491610.2:n.630C>A
ENST00000676607.1:n.966C>A
ENST00000676627.1:n.1400C>A
ENST00000676708.1:n.1950C>A
ENST00000676864.1:n.1819C>A
ENST00000677010.1:c.706C>A	ENSP00000503089.1:p.Arg236=
ENST00000677108.1:n.2576C>A
ENST00000677168.1:n.1142C>A
ENST00000677185.1:n.1233C>A
ENST00000677205.1:n.1454C>A
ENST00000677344.1:n.1944C>A
ENST00000677480.1:c.*347C>A	ENSP00000504378.1:n.*347C>A
ENST00000677519.1:n.1380C>A
ENST00000677593.1:n.1226C>A
ENST00000677740.1:n.2175C>A
ENST00000677991.1:n.1843C>A
ENST00000678001.1:n.1163C>A
ENST00000678085.1:n.1226C>A
ENST00000678177.1:n.2519C>A
ENST00000678603.1:n.1748C>A
ENST00000678724.1:c.595C>A	ENSP00000503874.1:p.Arg199=
ENST00000678920.1:n.828C>A
ENST00000679019.1:n.1440C>A
ENST00000679117.1:c.*485C>A	ENSP00000503240.1:n.*485C>A
ENST00000679339.1:n.1511C>A
ENST00000326739.8:c.670C>A	ENSP00000321584.4:p.Arg224=
ENST00000429182.5:c.464C>A
ENST00000442157.1:c.595C>A	ENSP00000403502.1:p.Arg199=
ENST00000462980.1:n.572C>A
ENST00000491610.1:n.630C>A
NM_000884.2:c.670C>A	NP_000875.2:p.Arg224=
XM_006713128.2:c.880C>A	XP_006713191.1:p.Arg294=
XM_006713128.3:c.880C>A	XP_006713191.1:p.Arg294=
XM_017006349.1:c.805C>A	XP_016861838.1:p.Arg269=
XM_017006350.1:c.805C>A	XP_016861839.1:p.Arg269=
NM_000884.3:c.670C>A MANE Select	NP_000875.2:p.Arg224=