Canonical Allele Identifier: CA352740613
Gene: IMPDH2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49026812C>T , CM000665.2:g.49026812C>T GRCh38
NC_000003.11:g.49064245C>T , CM000665.1:g.49064245C>T GRCh37
NC_000003.10:g.49039249C>T NCBI36
NG_012091.1:g.7631G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000703936.1:c.2734G>A ENSP00000515567.1:p.Asp912Asn
ENST00000703937.1:c.*1795G>A ENSP00000515568.1:n.*1795G>A
ENST00000326739.9:c.694G>A MANE Select ENSP00000321584.4:p.Asp232Asn
ENST00000429182.6:c.694G>A ENSP00000393525.2:p.Asp232Asn
ENST00000442157.2:c.619G>A ENSP00000403502.2:p.Asp207Asn
ENST00000462980.2:n.1209G>A
ENST00000472328.2:n.760G>A
ENST00000491610.2:n.654G>A
ENST00000676607.1:n.990G>A
ENST00000676627.1:n.1424G>A
ENST00000676708.1:n.1974G>A
ENST00000676864.1:n.1843G>A
ENST00000677010.1:c.730G>A ENSP00000503089.1:p.Asp244Asn
ENST00000677108.1:n.2600G>A
ENST00000677168.1:n.1166G>A
ENST00000677185.1:n.1257G>A
ENST00000677205.1:n.1478G>A
ENST00000677344.1:n.1968G>A
ENST00000677480.1:c.*371G>A ENSP00000504378.1:n.*371G>A
ENST00000677519.1:n.1404G>A
ENST00000677593.1:n.1250G>A
ENST00000677740.1:n.2199G>A
ENST00000677991.1:n.1867G>A
ENST00000678001.1:n.1187G>A
ENST00000678085.1:n.1250G>A
ENST00000678177.1:n.2543G>A
ENST00000678603.1:n.1772G>A
ENST00000678724.1:c.619G>A ENSP00000503874.1:p.Asp207Asn
ENST00000678920.1:n.852G>A
ENST00000679019.1:n.1464G>A
ENST00000679117.1:c.*509G>A ENSP00000503240.1:n.*509G>A
ENST00000679339.1:n.1535G>A
ENST00000326739.8:c.694G>A ENSP00000321584.4:p.Asp232Asn
ENST00000429182.5:c.488G>A
ENST00000442157.1:c.619G>A ENSP00000403502.1:p.Asp207Asn
ENST00000462980.1:n.596G>A
ENST00000491610.1:n.654G>A
NM_000884.2:c.694G>A NP_000875.2:p.Asp232Asn
XM_006713128.2:c.904G>A XP_006713191.1:p.Asp302Asn
XM_006713128.3:c.904G>A XP_006713191.1:p.Asp302Asn
XM_017006349.1:c.829G>A XP_016861838.1:p.Asp277Asn
XM_017006350.1:c.829G>A XP_016861839.1:p.Asp277Asn
NM_000884.3:c.694G>A MANE Select NP_000875.2:p.Asp232Asn