Canonical Allele Identifier: CA352741177
Gene: IMPDH2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49026874A>T , CM000665.2:g.49026874A>T GRCh38
NC_000003.11:g.49064307A>T , CM000665.1:g.49064307A>T GRCh37
NC_000003.10:g.49039311A>T NCBI36
NG_012091.1:g.7569T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000703936.1:c.2672T>A ENSP00000515567.1:p.Ile891Asn
ENST00000703937.1:c.*1733T>A ENSP00000515568.1:n.*1733T>A
ENST00000326739.9:c.632T>A MANE Select ENSP00000321584.4:p.Ile211Asn
ENST00000429182.6:c.632T>A ENSP00000393525.2:p.Ile211Asn
ENST00000442157.2:c.557T>A ENSP00000403502.2:p.Ile186Asn
ENST00000462980.2:n.1147T>A
ENST00000472328.2:n.698T>A
ENST00000491610.2:n.592T>A
ENST00000676607.1:n.928T>A
ENST00000676627.1:n.1362T>A
ENST00000676708.1:n.1912T>A
ENST00000676864.1:n.1781T>A
ENST00000677010.1:c.668T>A ENSP00000503089.1:p.Ile223Asn
ENST00000677108.1:n.2538T>A
ENST00000677168.1:n.1104T>A
ENST00000677185.1:n.1195T>A
ENST00000677205.1:n.1416T>A
ENST00000677344.1:n.1906T>A
ENST00000677480.1:c.*309T>A ENSP00000504378.1:n.*309T>A
ENST00000677519.1:n.1342T>A
ENST00000677593.1:n.1188T>A
ENST00000677740.1:n.2137T>A
ENST00000677991.1:n.1805T>A
ENST00000678001.1:n.1125T>A
ENST00000678085.1:n.1188T>A
ENST00000678177.1:n.2481T>A
ENST00000678603.1:n.1710T>A
ENST00000678724.1:c.557T>A ENSP00000503874.1:p.Ile186Asn
ENST00000678920.1:n.790T>A
ENST00000679019.1:n.1402T>A
ENST00000679117.1:c.*447T>A ENSP00000503240.1:n.*447T>A
ENST00000679339.1:n.1473T>A
ENST00000326739.8:c.632T>A ENSP00000321584.4:p.Ile211Asn
ENST00000429182.5:c.426T>A
ENST00000442157.1:c.557T>A ENSP00000403502.1:p.Ile186Asn
ENST00000462980.1:n.534T>A
ENST00000491610.1:n.592T>A
NM_000884.2:c.632T>A NP_000875.2:p.Ile211Asn
XM_006713128.2:c.842T>A XP_006713191.1:p.Ile281Asn
XM_006713128.3:c.842T>A XP_006713191.1:p.Ile281Asn
XM_017006349.1:c.767T>A XP_016861838.1:p.Ile256Asn
XM_017006350.1:c.767T>A XP_016861839.1:p.Ile256Asn
NM_000884.3:c.632T>A MANE Select NP_000875.2:p.Ile211Asn