Canonical Allele Identifier: CA352740626
Gene: IMPDH2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49026816A>C , CM000665.2:g.49026816A>C GRCh38
NC_000003.11:g.49064249A>C , CM000665.1:g.49064249A>C GRCh37
NC_000003.10:g.49039253A>C NCBI36
NG_012091.1:g.7627T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000703936.1:c.2730T>G ENSP00000515567.1:p.Asn910Lys
ENST00000703937.1:c.*1791T>G ENSP00000515568.1:n.*1791T>G
ENST00000326739.9:c.690T>G MANE Select ENSP00000321584.4:p.Asn230Lys
ENST00000429182.6:c.690T>G ENSP00000393525.2:p.Asn230Lys
ENST00000442157.2:c.615T>G ENSP00000403502.2:p.Asn205Lys
ENST00000462980.2:n.1205T>G
ENST00000472328.2:n.756T>G
ENST00000491610.2:n.650T>G
ENST00000676607.1:n.986T>G
ENST00000676627.1:n.1420T>G
ENST00000676708.1:n.1970T>G
ENST00000676864.1:n.1839T>G
ENST00000677010.1:c.726T>G ENSP00000503089.1:p.Asn242Lys
ENST00000677108.1:n.2596T>G
ENST00000677168.1:n.1162T>G
ENST00000677185.1:n.1253T>G
ENST00000677205.1:n.1474T>G
ENST00000677344.1:n.1964T>G
ENST00000677480.1:c.*367T>G ENSP00000504378.1:n.*367T>G
ENST00000677519.1:n.1400T>G
ENST00000677593.1:n.1246T>G
ENST00000677740.1:n.2195T>G
ENST00000677991.1:n.1863T>G
ENST00000678001.1:n.1183T>G
ENST00000678085.1:n.1246T>G
ENST00000678177.1:n.2539T>G
ENST00000678603.1:n.1768T>G
ENST00000678724.1:c.615T>G ENSP00000503874.1:p.Asn205Lys
ENST00000678920.1:n.848T>G
ENST00000679019.1:n.1460T>G
ENST00000679117.1:c.*505T>G ENSP00000503240.1:n.*505T>G
ENST00000679339.1:n.1531T>G
ENST00000326739.8:c.690T>G ENSP00000321584.4:p.Asn230Lys
ENST00000429182.5:c.484T>G
ENST00000442157.1:c.615T>G ENSP00000403502.1:p.Asn205Lys
ENST00000462980.1:n.592T>G
ENST00000491610.1:n.650T>G
NM_000884.2:c.690T>G NP_000875.2:p.Asn230Lys
XM_006713128.2:c.900T>G XP_006713191.1:p.Asn300Lys
XM_006713128.3:c.900T>G XP_006713191.1:p.Asn300Lys
XM_017006349.1:c.825T>G XP_016861838.1:p.Asn275Lys
XM_017006350.1:c.825T>G XP_016861839.1:p.Asn275Lys
NM_000884.3:c.690T>G MANE Select NP_000875.2:p.Asn230Lys