Canonical Allele Identifier: CA352741644
Gene: IMPDH2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49026977A>G , CM000665.2:g.49026977A>G GRCh38
NC_000003.11:g.49064410A>G , CM000665.1:g.49064410A>G GRCh37
NC_000003.10:g.49039414A>G NCBI36
NG_012091.1:g.7466T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000703936.1:c.2642T>C ENSP00000515567.1:p.Leu881Pro
ENST00000703937.1:c.*1703T>C ENSP00000515568.1:n.*1703T>C
ENST00000326739.9:c.602T>C MANE Select ENSP00000321584.4:p.Leu201Pro
ENST00000429182.6:c.602T>C ENSP00000393525.2:p.Leu201Pro
ENST00000442157.2:c.527T>C ENSP00000403502.2:p.Leu176Pro
ENST00000462980.2:n.1117T>C
ENST00000472328.2:n.668T>C
ENST00000491610.2:n.489T>C
ENST00000676607.1:n.898T>C
ENST00000676627.1:n.1332T>C
ENST00000676708.1:n.1809T>C
ENST00000676864.1:n.1678T>C
ENST00000677010.1:c.638T>C ENSP00000503089.1:p.Leu213Pro
ENST00000677108.1:n.2435T>C
ENST00000677168.1:n.1074T>C
ENST00000677185.1:n.1092T>C
ENST00000677205.1:n.1313T>C
ENST00000677344.1:n.1803T>C
ENST00000677480.1:c.*279T>C ENSP00000504378.1:n.*279T>C
ENST00000677519.1:n.1312T>C
ENST00000677593.1:n.1085T>C
ENST00000677740.1:n.2034T>C
ENST00000677991.1:n.1775T>C
ENST00000678001.1:n.1095T>C
ENST00000678085.1:n.1085T>C
ENST00000678177.1:n.2378T>C
ENST00000678603.1:n.1680T>C
ENST00000678724.1:c.527T>C ENSP00000503874.1:p.Leu176Pro
ENST00000678920.1:n.760T>C
ENST00000679019.1:n.1299T>C
ENST00000679117.1:c.*417T>C ENSP00000503240.1:n.*417T>C
ENST00000679339.1:n.1370T>C
ENST00000326739.8:c.602T>C ENSP00000321584.4:p.Leu201Pro
ENST00000429182.5:c.396T>C
ENST00000442157.1:c.527T>C ENSP00000403502.1:p.Leu176Pro
ENST00000462980.1:n.504T>C
ENST00000491610.1:n.489T>C
NM_000884.2:c.602T>C NP_000875.2:p.Leu201Pro
XM_006713128.2:c.812T>C XP_006713191.1:p.Leu271Pro
XM_006713128.3:c.812T>C XP_006713191.1:p.Leu271Pro
XM_017006349.1:c.737T>C XP_016861838.1:p.Leu246Pro
XM_017006350.1:c.737T>C XP_016861839.1:p.Leu246Pro
NM_000884.3:c.602T>C MANE Select NP_000875.2:p.Leu201Pro