Canonical Allele Identifier: CA352740715
Gene: IMPDH2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49026820T>C , CM000665.2:g.49026820T>C GRCh38
NC_000003.11:g.49064253T>C , CM000665.1:g.49064253T>C GRCh37
NC_000003.10:g.49039257T>C NCBI36
NG_012091.1:g.7623A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000703936.1:c.2726A>G ENSP00000515567.1:p.Lys909Arg
ENST00000703937.1:c.*1787A>G ENSP00000515568.1:n.*1787A>G
ENST00000326739.9:c.686A>G MANE Select ENSP00000321584.4:p.Lys229Arg
ENST00000429182.6:c.686A>G ENSP00000393525.2:p.Lys229Arg
ENST00000442157.2:c.611A>G ENSP00000403502.2:p.Lys204Arg
ENST00000462980.2:n.1201A>G
ENST00000472328.2:n.752A>G
ENST00000491610.2:n.646A>G
ENST00000676607.1:n.982A>G
ENST00000676627.1:n.1416A>G
ENST00000676708.1:n.1966A>G
ENST00000676864.1:n.1835A>G
ENST00000677010.1:c.722A>G ENSP00000503089.1:p.Lys241Arg
ENST00000677108.1:n.2592A>G
ENST00000677168.1:n.1158A>G
ENST00000677185.1:n.1249A>G
ENST00000677205.1:n.1470A>G
ENST00000677344.1:n.1960A>G
ENST00000677480.1:c.*363A>G ENSP00000504378.1:n.*363A>G
ENST00000677519.1:n.1396A>G
ENST00000677593.1:n.1242A>G
ENST00000677740.1:n.2191A>G
ENST00000677991.1:n.1859A>G
ENST00000678001.1:n.1179A>G
ENST00000678085.1:n.1242A>G
ENST00000678177.1:n.2535A>G
ENST00000678603.1:n.1764A>G
ENST00000678724.1:c.611A>G ENSP00000503874.1:p.Lys204Arg
ENST00000678920.1:n.844A>G
ENST00000679019.1:n.1456A>G
ENST00000679117.1:c.*501A>G ENSP00000503240.1:n.*501A>G
ENST00000679339.1:n.1527A>G
ENST00000326739.8:c.686A>G ENSP00000321584.4:p.Lys229Arg
ENST00000429182.5:c.480A>G
ENST00000442157.1:c.611A>G ENSP00000403502.1:p.Lys204Arg
ENST00000462980.1:n.588A>G
ENST00000491610.1:n.646A>G
NM_000884.2:c.686A>G NP_000875.2:p.Lys229Arg
XM_006713128.2:c.896A>G XP_006713191.1:p.Lys299Arg
XM_006713128.3:c.896A>G XP_006713191.1:p.Lys299Arg
XM_017006349.1:c.821A>G XP_016861838.1:p.Lys274Arg
XM_017006350.1:c.821A>G XP_016861839.1:p.Lys274Arg
NM_000884.3:c.686A>G MANE Select NP_000875.2:p.Lys229Arg