Canonical Allele Identifier: CA433629534

Gene: IMPDH2

Linked Data

• MyVariant Identifiers: chr3:g.49064183A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49026750A>C , CM000665.2:g.49026750A>C	GRCh38
NC_000003.11:g.49064183A>C , CM000665.1:g.49064183A>C	GRCh37
NC_000003.10:g.49039187A>C	NCBI36
NG_012091.1:g.7693T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703936.1:c.2796T>G	ENSP00000515567.1:p.Thr932=
ENST00000703937.1:c.*1857T>G	ENSP00000515568.1:n.*1857T>G
ENST00000326739.9:c.756T>G MANE Select	ENSP00000321584.4:p.Thr252=
ENST00000429182.6:c.756T>G	ENSP00000393525.2:p.Thr252=
ENST00000442157.2:c.681T>G	ENSP00000403502.2:p.Thr227=
ENST00000462980.2:n.1271T>G
ENST00000472328.2:n.822T>G
ENST00000491610.2:n.716T>G
ENST00000676607.1:n.1052T>G
ENST00000676627.1:n.1486T>G
ENST00000676708.1:n.2036T>G
ENST00000676864.1:n.1905T>G
ENST00000677010.1:c.792T>G	ENSP00000503089.1:p.Thr264=
ENST00000677108.1:n.2662T>G
ENST00000677168.1:n.1228T>G
ENST00000677185.1:n.1319T>G
ENST00000677205.1:n.1540T>G
ENST00000677344.1:n.2030T>G
ENST00000677480.1:c.*433T>G	ENSP00000504378.1:n.*433T>G
ENST00000677519.1:n.1466T>G
ENST00000677593.1:n.1312T>G
ENST00000677740.1:n.2261T>G
ENST00000677991.1:n.1929T>G
ENST00000678001.1:n.1249T>G
ENST00000678085.1:n.1312T>G
ENST00000678177.1:n.2605T>G
ENST00000678603.1:n.1834T>G
ENST00000678724.1:c.681T>G	ENSP00000503874.1:p.Thr227=
ENST00000678920.1:n.914T>G
ENST00000679019.1:n.1526T>G
ENST00000679117.1:c.*571T>G	ENSP00000503240.1:n.*571T>G
ENST00000679339.1:n.1597T>G
ENST00000326739.8:c.756T>G	ENSP00000321584.4:p.Thr252=
ENST00000429182.5:c.550T>G
ENST00000442157.1:c.681T>G	ENSP00000403502.1:p.Thr227=
ENST00000462980.1:n.658T>G
ENST00000491610.1:n.716T>G
NM_000884.2:c.756T>G	NP_000875.2:p.Thr252=
XM_006713128.2:c.966T>G	XP_006713191.1:p.Thr322=
XM_006713128.3:c.966T>G	XP_006713191.1:p.Thr322=
XM_017006349.1:c.891T>G	XP_016861838.1:p.Thr297=
XM_017006350.1:c.891T>G	XP_016861839.1:p.Thr297=
NM_000884.3:c.756T>G MANE Select	NP_000875.2:p.Thr252=