Canonical Allele Identifier: CA352741570
Gene: IMPDH2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49026969T>C , CM000665.2:g.49026969T>C GRCh38
NC_000003.11:g.49064402T>C , CM000665.1:g.49064402T>C GRCh37
NC_000003.10:g.49039406T>C NCBI36
NG_012091.1:g.7474A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000703936.1:c.2650A>G ENSP00000515567.1:p.Ser884Gly
ENST00000703937.1:c.*1711A>G ENSP00000515568.1:n.*1711A>G
ENST00000326739.9:c.610A>G MANE Select ENSP00000321584.4:p.Ser204Gly
ENST00000429182.6:c.610A>G ENSP00000393525.2:p.Ser204Gly
ENST00000442157.2:c.535A>G ENSP00000403502.2:p.Ser179Gly
ENST00000462980.2:n.1125A>G
ENST00000472328.2:n.676A>G
ENST00000491610.2:n.497A>G
ENST00000676607.1:n.906A>G
ENST00000676627.1:n.1340A>G
ENST00000676708.1:n.1817A>G
ENST00000676864.1:n.1686A>G
ENST00000677010.1:c.646A>G ENSP00000503089.1:p.Ser216Gly
ENST00000677108.1:n.2443A>G
ENST00000677168.1:n.1082A>G
ENST00000677185.1:n.1100A>G
ENST00000677205.1:n.1321A>G
ENST00000677344.1:n.1811A>G
ENST00000677480.1:c.*287A>G ENSP00000504378.1:n.*287A>G
ENST00000677519.1:n.1320A>G
ENST00000677593.1:n.1093A>G
ENST00000677740.1:n.2042A>G
ENST00000677991.1:n.1783A>G
ENST00000678001.1:n.1103A>G
ENST00000678085.1:n.1093A>G
ENST00000678177.1:n.2386A>G
ENST00000678603.1:n.1688A>G
ENST00000678724.1:c.535A>G ENSP00000503874.1:p.Ser179Gly
ENST00000678920.1:n.768A>G
ENST00000679019.1:n.1307A>G
ENST00000679117.1:c.*425A>G ENSP00000503240.1:n.*425A>G
ENST00000679339.1:n.1378A>G
ENST00000326739.8:c.610A>G ENSP00000321584.4:p.Ser204Gly
ENST00000429182.5:c.404A>G
ENST00000442157.1:c.535A>G ENSP00000403502.1:p.Ser179Gly
ENST00000462980.1:n.512A>G
ENST00000491610.1:n.497A>G
NM_000884.2:c.610A>G NP_000875.2:p.Ser204Gly
XM_006713128.2:c.820A>G XP_006713191.1:p.Ser274Gly
XM_006713128.3:c.820A>G XP_006713191.1:p.Ser274Gly
XM_017006349.1:c.745A>G XP_016861838.1:p.Ser249Gly
XM_017006350.1:c.745A>G XP_016861839.1:p.Ser249Gly
NM_000884.3:c.610A>G MANE Select NP_000875.2:p.Ser204Gly