Canonical Allele Identifier: CA2390651

Gene: IMPDH2

Linked Data

• dbSNP Id: rs769438849
• ExAC: 3:49064384 A / G
• gnomAD v2: 3-49064384-A-G
• gnomAD v4: 3-49026951-A-G
• MyVariant Identifiers: chr3:g.49064384A>G (hg19) ; chr3:g.49026951A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49026951A>G , CM000665.2:g.49026951A>G	GRCh38
NC_000003.11:g.49064384A>G , CM000665.1:g.49064384A>G	GRCh37
NC_000003.10:g.49039388A>G	NCBI36
NG_012091.1:g.7492T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703936.1:c.2659+9T>C	ENSP00000515567.1:n.2659+9T>C
ENST00000703937.1:c.*1720+9T>C	ENSP00000515568.1:n.*1720+9T>C
ENST00000326739.9:c.619+9T>C MANE Select	ENSP00000321584.4:n.619+9T>C
ENST00000429182.6:c.619+9T>C	ENSP00000393525.2:n.619+9T>C
ENST00000442157.2:c.544+9T>C	ENSP00000403502.2:n.544+9T>C
ENST00000462980.2:n.1134+9T>C
ENST00000472328.2:n.685+9T>C
ENST00000491610.2:n.515T>C
ENST00000676607.1:n.915+9T>C
ENST00000676627.1:n.1349+9T>C
ENST00000676708.1:n.1835T>C
ENST00000676864.1:n.1704T>C
ENST00000677010.1:c.655+9T>C	ENSP00000503089.1:n.655+9T>C
ENST00000677108.1:n.2461T>C
ENST00000677168.1:n.1091+9T>C
ENST00000677185.1:n.1118T>C
ENST00000677205.1:n.1339T>C
ENST00000677344.1:n.1829T>C
ENST00000677480.1:c.*296+9T>C	ENSP00000504378.1:n.*296+9T>C
ENST00000677519.1:n.1329+9T>C
ENST00000677593.1:n.1111T>C
ENST00000677740.1:n.2060T>C
ENST00000677991.1:n.1792+9T>C
ENST00000678001.1:n.1112+9T>C
ENST00000678085.1:n.1111T>C
ENST00000678177.1:n.2404T>C
ENST00000678603.1:n.1697+9T>C
ENST00000678724.1:c.544+9T>C	ENSP00000503874.1:n.544+9T>C
ENST00000678920.1:n.777+9T>C
ENST00000679019.1:n.1325T>C
ENST00000679117.1:c.*434+9T>C	ENSP00000503240.1:n.*434+9T>C
ENST00000679339.1:n.1396T>C
ENST00000326739.8:c.619+9T>C	ENSP00000321584.4:n.619+9T>C
ENST00000429182.5:c.413+9T>C
ENST00000442157.1:c.544+9T>C	ENSP00000403502.1:n.544+9T>C
ENST00000462980.1:n.521+9T>C
ENST00000491610.1:n.515T>C
NM_000884.2:c.619+9T>C	NP_000875.2:n.619+9T>C
XM_006713128.2:c.829+9T>C	XP_006713191.1:n.829+9T>C
XM_006713128.3:c.829+9T>C	XP_006713191.1:n.829+9T>C
XM_017006349.1:c.754+9T>C	XP_016861838.1:n.754+9T>C
XM_017006350.1:c.754+9T>C	XP_016861839.1:n.754+9T>C
NM_000884.3:c.619+9T>C MANE Select	NP_000875.2:n.619+9T>C