Canonical Allele Identifier: CA2665685812

Gene: IMPDH2

Linked Data

• gnomAD v4: 3-49026941-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49026941T>C , CM000665.2:g.49026941T>C	GRCh38
NC_000003.11:g.49064374T>C , CM000665.1:g.49064374T>C	GRCh37
NC_000003.10:g.49039378T>C	NCBI36
NG_012091.1:g.7502A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703936.1:c.2659+19A>G	ENSP00000515567.1:n.2659+19A>G
ENST00000703937.1:c.*1720+19A>G	ENSP00000515568.1:n.*1720+19A>G
ENST00000326739.9:c.619+19A>G MANE Select	ENSP00000321584.4:n.619+19A>G
ENST00000429182.6:c.619+19A>G	ENSP00000393525.2:n.619+19A>G
ENST00000442157.2:c.544+19A>G	ENSP00000403502.2:n.544+19A>G
ENST00000462980.2:n.1134+19A>G
ENST00000472328.2:n.685+19A>G
ENST00000491610.2:n.525A>G
ENST00000676607.1:n.915+19A>G
ENST00000676627.1:n.1349+19A>G
ENST00000676708.1:n.1845A>G
ENST00000676864.1:n.1714A>G
ENST00000677010.1:c.655+19A>G	ENSP00000503089.1:n.655+19A>G
ENST00000677108.1:n.2471A>G
ENST00000677168.1:n.1091+19A>G
ENST00000677185.1:n.1128A>G
ENST00000677205.1:n.1349A>G
ENST00000677344.1:n.1839A>G
ENST00000677480.1:c.*296+19A>G	ENSP00000504378.1:n.*296+19A>G
ENST00000677519.1:n.1329+19A>G
ENST00000677593.1:n.1121A>G
ENST00000677740.1:n.2070A>G
ENST00000677991.1:n.1792+19A>G
ENST00000678001.1:n.1112+19A>G
ENST00000678085.1:n.1121A>G
ENST00000678177.1:n.2414A>G
ENST00000678603.1:n.1697+19A>G
ENST00000678724.1:c.544+19A>G	ENSP00000503874.1:n.544+19A>G
ENST00000678920.1:n.777+19A>G
ENST00000679019.1:n.1335A>G
ENST00000679117.1:c.*434+19A>G	ENSP00000503240.1:n.*434+19A>G
ENST00000679339.1:n.1406A>G
ENST00000326739.8:c.619+19A>G	ENSP00000321584.4:n.619+19A>G
ENST00000429182.5:c.413+19A>G
ENST00000442157.1:c.544+19A>G	ENSP00000403502.1:n.544+19A>G
ENST00000462980.1:n.521+19A>G
ENST00000491610.1:n.525A>G
NM_000884.2:c.619+19A>G	NP_000875.2:n.619+19A>G
XM_006713128.2:c.829+19A>G	XP_006713191.1:n.829+19A>G
XM_006713128.3:c.829+19A>G	XP_006713191.1:n.829+19A>G
XM_017006349.1:c.754+19A>G	XP_016861838.1:n.754+19A>G
XM_017006350.1:c.754+19A>G	XP_016861839.1:n.754+19A>G
NM_000884.3:c.619+19A>G MANE Select	NP_000875.2:n.619+19A>G