Canonical Allele Identifier: CA352739883
Gene: IMPDH2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49026706C>T , CM000665.2:g.49026706C>T GRCh38
NC_000003.11:g.49064139C>T , CM000665.1:g.49064139C>T GRCh37
NC_000003.10:g.49039143C>T NCBI36
NG_012091.1:g.7737G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000703936.1:c.2840G>A ENSP00000515567.1:p.Gly947Asp
ENST00000703937.1:c.*1901G>A ENSP00000515568.1:n.*1901G>A
ENST00000326739.9:c.800G>A MANE Select ENSP00000321584.4:p.Gly267Asp
ENST00000429182.6:c.800G>A ENSP00000393525.2:p.Gly267Asp
ENST00000442157.2:c.725G>A ENSP00000403502.2:p.Gly242Asp
ENST00000462980.2:n.1315G>A
ENST00000472328.2:n.866G>A
ENST00000491610.2:n.760G>A
ENST00000676607.1:n.1096G>A
ENST00000676627.1:n.1530G>A
ENST00000676708.1:n.2080G>A
ENST00000676864.1:n.1949G>A
ENST00000677010.1:c.836G>A ENSP00000503089.1:p.Gly279Asp
ENST00000677108.1:n.2706G>A
ENST00000677168.1:n.1272G>A
ENST00000677185.1:n.1363G>A
ENST00000677205.1:n.1584G>A
ENST00000677344.1:n.2074G>A
ENST00000677480.1:c.*477G>A ENSP00000504378.1:n.*477G>A
ENST00000677519.1:n.1510G>A
ENST00000677593.1:n.1356G>A
ENST00000677740.1:n.2305G>A
ENST00000677991.1:n.1973G>A
ENST00000678001.1:n.1293G>A
ENST00000678085.1:n.1356G>A
ENST00000678177.1:n.2649G>A
ENST00000678603.1:n.1878G>A
ENST00000678724.1:c.725G>A ENSP00000503874.1:p.Gly242Asp
ENST00000678920.1:n.958G>A
ENST00000679019.1:n.1570G>A
ENST00000679117.1:c.*615G>A ENSP00000503240.1:n.*615G>A
ENST00000679339.1:n.1641G>A
ENST00000326739.8:c.800G>A ENSP00000321584.4:p.Gly267Asp
ENST00000429182.5:c.594G>A
ENST00000442157.1:c.725G>A ENSP00000403502.1:p.Gly242Asp
ENST00000462980.1:n.702G>A
ENST00000491610.1:n.760G>A
NM_000884.2:c.800G>A NP_000875.2:p.Gly267Asp
XM_006713128.2:c.1010G>A XP_006713191.1:p.Gly337Asp
XM_006713128.3:c.1010G>A XP_006713191.1:p.Gly337Asp
XM_017006349.1:c.935G>A XP_016861838.1:p.Gly312Asp
XM_017006350.1:c.935G>A XP_016861839.1:p.Gly312Asp
NM_000884.3:c.800G>A MANE Select NP_000875.2:p.Gly267Asp