Canonical Allele Identifier: CA352740658
Gene: IMPDH2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49026818T>C , CM000665.2:g.49026818T>C GRCh38
NC_000003.11:g.49064251T>C , CM000665.1:g.49064251T>C GRCh37
NC_000003.10:g.49039255T>C NCBI36
NG_012091.1:g.7625A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000703936.1:c.2728A>G ENSP00000515567.1:p.Asn910Asp
ENST00000703937.1:c.*1789A>G ENSP00000515568.1:n.*1789A>G
ENST00000326739.9:c.688A>G MANE Select ENSP00000321584.4:p.Asn230Asp
ENST00000429182.6:c.688A>G ENSP00000393525.2:p.Asn230Asp
ENST00000442157.2:c.613A>G ENSP00000403502.2:p.Asn205Asp
ENST00000462980.2:n.1203A>G
ENST00000472328.2:n.754A>G
ENST00000491610.2:n.648A>G
ENST00000676607.1:n.984A>G
ENST00000676627.1:n.1418A>G
ENST00000676708.1:n.1968A>G
ENST00000676864.1:n.1837A>G
ENST00000677010.1:c.724A>G ENSP00000503089.1:p.Asn242Asp
ENST00000677108.1:n.2594A>G
ENST00000677168.1:n.1160A>G
ENST00000677185.1:n.1251A>G
ENST00000677205.1:n.1472A>G
ENST00000677344.1:n.1962A>G
ENST00000677480.1:c.*365A>G ENSP00000504378.1:n.*365A>G
ENST00000677519.1:n.1398A>G
ENST00000677593.1:n.1244A>G
ENST00000677740.1:n.2193A>G
ENST00000677991.1:n.1861A>G
ENST00000678001.1:n.1181A>G
ENST00000678085.1:n.1244A>G
ENST00000678177.1:n.2537A>G
ENST00000678603.1:n.1766A>G
ENST00000678724.1:c.613A>G ENSP00000503874.1:p.Asn205Asp
ENST00000678920.1:n.846A>G
ENST00000679019.1:n.1458A>G
ENST00000679117.1:c.*503A>G ENSP00000503240.1:n.*503A>G
ENST00000679339.1:n.1529A>G
ENST00000326739.8:c.688A>G ENSP00000321584.4:p.Asn230Asp
ENST00000429182.5:c.482A>G
ENST00000442157.1:c.613A>G ENSP00000403502.1:p.Asn205Asp
ENST00000462980.1:n.590A>G
ENST00000491610.1:n.648A>G
NM_000884.2:c.688A>G NP_000875.2:p.Asn230Asp
XM_006713128.2:c.898A>G XP_006713191.1:p.Asn300Asp
XM_006713128.3:c.898A>G XP_006713191.1:p.Asn300Asp
XM_017006349.1:c.823A>G XP_016861838.1:p.Asn275Asp
XM_017006350.1:c.823A>G XP_016861839.1:p.Asn275Asp
NM_000884.3:c.688A>G MANE Select NP_000875.2:p.Asn230Asp