Canonical Allele Identifier: CA352739652
Gene: IMPDH2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49026594T>C , CM000665.2:g.49026594T>C GRCh38
NC_000003.11:g.49064027T>C , CM000665.1:g.49064027T>C GRCh37
NC_000003.10:g.49039031T>C NCBI36
NG_012091.1:g.7849A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000703936.1:c.2875A>G ENSP00000515567.1:p.Asn959Asp
ENST00000703937.1:c.*1936A>G ENSP00000515568.1:n.*1936A>G
ENST00000326739.9:c.835A>G MANE Select ENSP00000321584.4:p.Asn279Asp
ENST00000429182.6:c.835A>G ENSP00000393525.2:p.Asn279Asp
ENST00000442157.2:c.760A>G ENSP00000403502.2:p.Asn254Asp
ENST00000462980.2:n.1350A>G
ENST00000472328.2:n.901A>G
ENST00000491610.2:n.795A>G
ENST00000676607.1:n.1131A>G
ENST00000676627.1:n.1565A>G
ENST00000676708.1:n.2115A>G
ENST00000676864.1:n.1984A>G
ENST00000677010.1:c.859A>G ENSP00000503089.1:p.Asn287Asp
ENST00000677108.1:n.2818A>G
ENST00000677168.1:n.1307A>G
ENST00000677185.1:n.1398A>G
ENST00000677205.1:n.1619A>G
ENST00000677344.1:n.2109A>G
ENST00000677480.1:c.*512A>G ENSP00000504378.1:n.*512A>G
ENST00000677519.1:n.1545A>G
ENST00000677593.1:n.1391A>G
ENST00000677740.1:n.2340A>G
ENST00000677991.1:n.2008A>G
ENST00000678001.1:n.1328A>G
ENST00000678085.1:n.1468A>G
ENST00000678177.1:n.2761A>G
ENST00000678603.1:n.1913A>G
ENST00000678724.1:c.760A>G ENSP00000503874.1:p.Asn254Asp
ENST00000678920.1:n.993A>G
ENST00000679019.1:n.1682A>G
ENST00000679117.1:c.*650A>G ENSP00000503240.1:n.*650A>G
ENST00000679339.1:n.1676A>G
ENST00000326739.8:c.835A>G ENSP00000321584.4:p.Asn279Asp
ENST00000429182.5:c.629A>G
ENST00000442157.1:c.760A>G ENSP00000403502.1:p.Asn254Asp
ENST00000462980.1:n.737A>G
ENST00000491610.1:n.795A>G
NM_000884.2:c.835A>G NP_000875.2:p.Asn279Asp
XM_006713128.2:c.1045A>G XP_006713191.1:p.Asn349Asp
XM_006713128.3:c.1045A>G XP_006713191.1:p.Asn349Asp
XM_017006349.1:c.970A>G XP_016861838.1:p.Asn324Asp
XM_017006350.1:c.970A>G XP_016861839.1:p.Asn324Asp
NM_000884.3:c.835A>G MANE Select NP_000875.2:p.Asn279Asp