Canonical Allele Identifier: CA352740979
Gene: IMPDH2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49026861A>T , CM000665.2:g.49026861A>T GRCh38
NC_000003.11:g.49064294A>T , CM000665.1:g.49064294A>T GRCh37
NC_000003.10:g.49039298A>T NCBI36
NG_012091.1:g.7582T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000703936.1:c.2685T>A ENSP00000515567.1:p.Asp895Glu
ENST00000703937.1:c.*1746T>A ENSP00000515568.1:n.*1746T>A
ENST00000326739.9:c.645T>A MANE Select ENSP00000321584.4:p.Asp215Glu
ENST00000429182.6:c.645T>A ENSP00000393525.2:p.Asp215Glu
ENST00000442157.2:c.570T>A ENSP00000403502.2:p.Asp190Glu
ENST00000462980.2:n.1160T>A
ENST00000472328.2:n.711T>A
ENST00000491610.2:n.605T>A
ENST00000676607.1:n.941T>A
ENST00000676627.1:n.1375T>A
ENST00000676708.1:n.1925T>A
ENST00000676864.1:n.1794T>A
ENST00000677010.1:c.681T>A ENSP00000503089.1:p.Asp227Glu
ENST00000677108.1:n.2551T>A
ENST00000677168.1:n.1117T>A
ENST00000677185.1:n.1208T>A
ENST00000677205.1:n.1429T>A
ENST00000677344.1:n.1919T>A
ENST00000677480.1:c.*322T>A ENSP00000504378.1:n.*322T>A
ENST00000677519.1:n.1355T>A
ENST00000677593.1:n.1201T>A
ENST00000677740.1:n.2150T>A
ENST00000677991.1:n.1818T>A
ENST00000678001.1:n.1138T>A
ENST00000678085.1:n.1201T>A
ENST00000678177.1:n.2494T>A
ENST00000678603.1:n.1723T>A
ENST00000678724.1:c.570T>A ENSP00000503874.1:p.Asp190Glu
ENST00000678920.1:n.803T>A
ENST00000679019.1:n.1415T>A
ENST00000679117.1:c.*460T>A ENSP00000503240.1:n.*460T>A
ENST00000679339.1:n.1486T>A
ENST00000326739.8:c.645T>A ENSP00000321584.4:p.Asp215Glu
ENST00000429182.5:c.439T>A
ENST00000442157.1:c.570T>A ENSP00000403502.1:p.Asp190Glu
ENST00000462980.1:n.547T>A
ENST00000491610.1:n.605T>A
NM_000884.2:c.645T>A NP_000875.2:p.Asp215Glu
XM_006713128.2:c.855T>A XP_006713191.1:p.Asp285Glu
XM_006713128.3:c.855T>A XP_006713191.1:p.Asp285Glu
XM_017006349.1:c.780T>A XP_016861838.1:p.Asp260Glu
XM_017006350.1:c.780T>A XP_016861839.1:p.Asp260Glu
NM_000884.3:c.645T>A MANE Select NP_000875.2:p.Asp215Glu