Canonical Allele Identifier: CA1363291728
Gene: IMPDH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49026931C= , CM000665.2:g.49026931C= GRCh38
NC_000003.11:g.49064364C= , CM000665.1:g.49064364C= GRCh37
NC_000003.10:g.49039368C= NCBI36
NG_012091.1:g.7512G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000703936.1:c.2659+29G= ENSP00000515567.1:n.2659+29G=
ENST00000703937.1:c.*1720+29G= ENSP00000515568.1:n.*1720+29G=
ENST00000326739.9:c.619+29G= MANE Select ENSP00000321584.4:n.619+29G=
ENST00000429182.6:c.619+29G= ENSP00000393525.2:n.619+29G=
ENST00000442157.2:c.544+29G= ENSP00000403502.2:n.544+29G=
ENST00000462980.2:n.1134+29G=
ENST00000472328.2:n.685+29G=
ENST00000491610.2:n.535G=
ENST00000676607.1:n.915+29G=
ENST00000676627.1:n.1349+29G=
ENST00000676708.1:n.1855G=
ENST00000676864.1:n.1724G=
ENST00000677010.1:c.655+29G= ENSP00000503089.1:n.655+29G=
ENST00000677108.1:n.2481G=
ENST00000677168.1:n.1091+29G=
ENST00000677185.1:n.1138G=
ENST00000677205.1:n.1359G=
ENST00000677344.1:n.1849G=
ENST00000677480.1:c.*296+29G= ENSP00000504378.1:n.*296+29G=
ENST00000677519.1:n.1329+29G=
ENST00000677593.1:n.1131G=
ENST00000677740.1:n.2080G=
ENST00000677991.1:n.1792+29G=
ENST00000678001.1:n.1112+29G=
ENST00000678085.1:n.1131G=
ENST00000678177.1:n.2424G=
ENST00000678603.1:n.1697+29G=
ENST00000678724.1:c.544+29G= ENSP00000503874.1:n.544+29G=
ENST00000678920.1:n.777+29G=
ENST00000679019.1:n.1345G=
ENST00000679117.1:c.*434+29G= ENSP00000503240.1:n.*434+29G=
ENST00000679339.1:n.1416G=
ENST00000326739.8:c.619+29G= ENSP00000321584.4:n.619+29G=
ENST00000429182.5:c.413+29G=
ENST00000442157.1:c.544+29G= ENSP00000403502.1:n.544+29G=
ENST00000462980.1:n.521+29G=
ENST00000491610.1:n.535G=
NM_000884.2:c.619+29G= NP_000875.2:n.619+29G=
XM_006713128.2:c.829+29G= XP_006713191.1:n.829+29G=
XM_006713128.3:c.829+29G= XP_006713191.1:n.829+29G=
XM_017006349.1:c.754+29G= XP_016861838.1:n.754+29G=
XM_017006350.1:c.754+29G= XP_016861839.1:n.754+29G=
NM_000884.3:c.619+29G= MANE Select NP_000875.2:n.619+29G=