Canonical Allele Identifier: CA2665685801
Gene: IMPDH2 HGNC NCBI

Linked Data

gnomAD v4: 3-49026893-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49026893T>C , CM000665.2:g.49026893T>C GRCh38
NC_000003.11:g.49064326T>C , CM000665.1:g.49064326T>C GRCh37
NC_000003.10:g.49039330T>C NCBI36
NG_012091.1:g.7550A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000703936.1:c.2660-7A>G ENSP00000515567.1:n.2660-7A>G
ENST00000703937.1:c.*1721-7A>G ENSP00000515568.1:n.*1721-7A>G
ENST00000326739.9:c.620-7A>G MANE Select ENSP00000321584.4:n.620-7A>G
ENST00000429182.6:c.620-7A>G ENSP00000393525.2:n.620-7A>G
ENST00000442157.2:c.545-7A>G ENSP00000403502.2:n.545-7A>G
ENST00000462980.2:n.1135-7A>G
ENST00000472328.2:n.686-7A>G
ENST00000491610.2:n.573A>G
ENST00000676607.1:n.916-7A>G
ENST00000676627.1:n.1350-7A>G
ENST00000676708.1:n.1893A>G
ENST00000676864.1:n.1762A>G
ENST00000677010.1:c.656-7A>G ENSP00000503089.1:n.656-7A>G
ENST00000677108.1:n.2519A>G
ENST00000677168.1:n.1092-7A>G
ENST00000677185.1:n.1176A>G
ENST00000677205.1:n.1397A>G
ENST00000677344.1:n.1887A>G
ENST00000677480.1:c.*297-7A>G ENSP00000504378.1:n.*297-7A>G
ENST00000677519.1:n.1330-7A>G
ENST00000677593.1:n.1169A>G
ENST00000677740.1:n.2118A>G
ENST00000677991.1:n.1793-7A>G
ENST00000678001.1:n.1113-7A>G
ENST00000678085.1:n.1169A>G
ENST00000678177.1:n.2462A>G
ENST00000678603.1:n.1698-7A>G
ENST00000678724.1:c.545-7A>G ENSP00000503874.1:n.545-7A>G
ENST00000678920.1:n.778-7A>G
ENST00000679019.1:n.1383A>G
ENST00000679117.1:c.*435-7A>G ENSP00000503240.1:n.*435-7A>G
ENST00000679339.1:n.1454A>G
ENST00000326739.8:c.620-7A>G ENSP00000321584.4:n.620-7A>G
ENST00000429182.5:c.414-7A>G
ENST00000442157.1:c.545-7A>G ENSP00000403502.1:n.545-7A>G
ENST00000462980.1:n.522-7A>G
ENST00000491610.1:n.573A>G
NM_000884.2:c.620-7A>G NP_000875.2:n.620-7A>G
XM_006713128.2:c.830-7A>G XP_006713191.1:n.830-7A>G
XM_006713128.3:c.830-7A>G XP_006713191.1:n.830-7A>G
XM_017006349.1:c.755-7A>G XP_016861838.1:n.755-7A>G
XM_017006350.1:c.755-7A>G XP_016861839.1:n.755-7A>G
NM_000884.3:c.620-7A>G MANE Select NP_000875.2:n.620-7A>G