Canonical Allele Identifier: CA352740530
Gene: IMPDH2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49026800C>G , CM000665.2:g.49026800C>G GRCh38
NC_000003.11:g.49064233C>G , CM000665.1:g.49064233C>G GRCh37
NC_000003.10:g.49039237C>G NCBI36
NG_012091.1:g.7643G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000703936.1:c.2746G>C ENSP00000515567.1:p.Ala916Pro
ENST00000703937.1:c.*1807G>C ENSP00000515568.1:n.*1807G>C
ENST00000326739.9:c.706G>C MANE Select ENSP00000321584.4:p.Ala236Pro
ENST00000429182.6:c.706G>C ENSP00000393525.2:p.Ala236Pro
ENST00000442157.2:c.631G>C ENSP00000403502.2:p.Ala211Pro
ENST00000462980.2:n.1221G>C
ENST00000472328.2:n.772G>C
ENST00000491610.2:n.666G>C
ENST00000676607.1:n.1002G>C
ENST00000676627.1:n.1436G>C
ENST00000676708.1:n.1986G>C
ENST00000676864.1:n.1855G>C
ENST00000677010.1:c.742G>C ENSP00000503089.1:p.Ala248Pro
ENST00000677108.1:n.2612G>C
ENST00000677168.1:n.1178G>C
ENST00000677185.1:n.1269G>C
ENST00000677205.1:n.1490G>C
ENST00000677344.1:n.1980G>C
ENST00000677480.1:c.*383G>C ENSP00000504378.1:n.*383G>C
ENST00000677519.1:n.1416G>C
ENST00000677593.1:n.1262G>C
ENST00000677740.1:n.2211G>C
ENST00000677991.1:n.1879G>C
ENST00000678001.1:n.1199G>C
ENST00000678085.1:n.1262G>C
ENST00000678177.1:n.2555G>C
ENST00000678603.1:n.1784G>C
ENST00000678724.1:c.631G>C ENSP00000503874.1:p.Ala211Pro
ENST00000678920.1:n.864G>C
ENST00000679019.1:n.1476G>C
ENST00000679117.1:c.*521G>C ENSP00000503240.1:n.*521G>C
ENST00000679339.1:n.1547G>C
ENST00000326739.8:c.706G>C ENSP00000321584.4:p.Ala236Pro
ENST00000429182.5:c.500G>C
ENST00000442157.1:c.631G>C ENSP00000403502.1:p.Ala211Pro
ENST00000462980.1:n.608G>C
ENST00000491610.1:n.666G>C
NM_000884.2:c.706G>C NP_000875.2:p.Ala236Pro
XM_006713128.2:c.916G>C XP_006713191.1:p.Ala306Pro
XM_006713128.3:c.916G>C XP_006713191.1:p.Ala306Pro
XM_017006349.1:c.841G>C XP_016861838.1:p.Ala281Pro
XM_017006350.1:c.841G>C XP_016861839.1:p.Ala281Pro
NM_000884.3:c.706G>C MANE Select NP_000875.2:p.Ala236Pro