Canonical Allele Identifier: CA352739936
Gene: IMPDH2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49026713G>C , CM000665.2:g.49026713G>C GRCh38
NC_000003.11:g.49064146G>C , CM000665.1:g.49064146G>C GRCh37
NC_000003.10:g.49039150G>C NCBI36
NG_012091.1:g.7730C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000703936.1:c.2833C>G ENSP00000515567.1:p.Gln945Glu
ENST00000703937.1:c.*1894C>G ENSP00000515568.1:n.*1894C>G
ENST00000326739.9:c.793C>G MANE Select ENSP00000321584.4:p.Gln265Glu
ENST00000429182.6:c.793C>G ENSP00000393525.2:p.Gln265Glu
ENST00000442157.2:c.718C>G ENSP00000403502.2:p.Gln240Glu
ENST00000462980.2:n.1308C>G
ENST00000472328.2:n.859C>G
ENST00000491610.2:n.753C>G
ENST00000676607.1:n.1089C>G
ENST00000676627.1:n.1523C>G
ENST00000676708.1:n.2073C>G
ENST00000676864.1:n.1942C>G
ENST00000677010.1:c.829C>G ENSP00000503089.1:p.Gln277Glu
ENST00000677108.1:n.2699C>G
ENST00000677168.1:n.1265C>G
ENST00000677185.1:n.1356C>G
ENST00000677205.1:n.1577C>G
ENST00000677344.1:n.2067C>G
ENST00000677480.1:c.*470C>G ENSP00000504378.1:n.*470C>G
ENST00000677519.1:n.1503C>G
ENST00000677593.1:n.1349C>G
ENST00000677740.1:n.2298C>G
ENST00000677991.1:n.1966C>G
ENST00000678001.1:n.1286C>G
ENST00000678085.1:n.1349C>G
ENST00000678177.1:n.2642C>G
ENST00000678603.1:n.1871C>G
ENST00000678724.1:c.718C>G ENSP00000503874.1:p.Gln240Glu
ENST00000678920.1:n.951C>G
ENST00000679019.1:n.1563C>G
ENST00000679117.1:c.*608C>G ENSP00000503240.1:n.*608C>G
ENST00000679339.1:n.1634C>G
ENST00000326739.8:c.793C>G ENSP00000321584.4:p.Gln265Glu
ENST00000429182.5:c.587C>G
ENST00000442157.1:c.718C>G ENSP00000403502.1:p.Gln240Glu
ENST00000462980.1:n.695C>G
ENST00000491610.1:n.753C>G
NM_000884.2:c.793C>G NP_000875.2:p.Gln265Glu
XM_006713128.2:c.1003C>G XP_006713191.1:p.Gln335Glu
XM_006713128.3:c.1003C>G XP_006713191.1:p.Gln335Glu
XM_017006349.1:c.928C>G XP_016861838.1:p.Gln310Glu
XM_017006350.1:c.928C>G XP_016861839.1:p.Gln310Glu
NM_000884.3:c.793C>G MANE Select NP_000875.2:p.Gln265Glu