Canonical Allele Identifier: CA433629648

Gene: IMPDH2

Linked Data

• MyVariant Identifiers: chr3:g.49064267C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49026834C>G , CM000665.2:g.49026834C>G	GRCh38
NC_000003.11:g.49064267C>G , CM000665.1:g.49064267C>G	GRCh37
NC_000003.10:g.49039271C>G	NCBI36
NG_012091.1:g.7609G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703936.1:c.2712G>C	ENSP00000515567.1:p.Arg904=
ENST00000703937.1:c.*1773G>C	ENSP00000515568.1:n.*1773G>C
ENST00000326739.9:c.672G>C MANE Select	ENSP00000321584.4:p.Arg224=
ENST00000429182.6:c.672G>C	ENSP00000393525.2:p.Arg224=
ENST00000442157.2:c.597G>C	ENSP00000403502.2:p.Arg199=
ENST00000462980.2:n.1187G>C
ENST00000472328.2:n.738G>C
ENST00000491610.2:n.632G>C
ENST00000676607.1:n.968G>C
ENST00000676627.1:n.1402G>C
ENST00000676708.1:n.1952G>C
ENST00000676864.1:n.1821G>C
ENST00000677010.1:c.708G>C	ENSP00000503089.1:p.Arg236=
ENST00000677108.1:n.2578G>C
ENST00000677168.1:n.1144G>C
ENST00000677185.1:n.1235G>C
ENST00000677205.1:n.1456G>C
ENST00000677344.1:n.1946G>C
ENST00000677480.1:c.*349G>C	ENSP00000504378.1:n.*349G>C
ENST00000677519.1:n.1382G>C
ENST00000677593.1:n.1228G>C
ENST00000677740.1:n.2177G>C
ENST00000677991.1:n.1845G>C
ENST00000678001.1:n.1165G>C
ENST00000678085.1:n.1228G>C
ENST00000678177.1:n.2521G>C
ENST00000678603.1:n.1750G>C
ENST00000678724.1:c.597G>C	ENSP00000503874.1:p.Arg199=
ENST00000678920.1:n.830G>C
ENST00000679019.1:n.1442G>C
ENST00000679117.1:c.*487G>C	ENSP00000503240.1:n.*487G>C
ENST00000679339.1:n.1513G>C
ENST00000326739.8:c.672G>C	ENSP00000321584.4:p.Arg224=
ENST00000429182.5:c.466G>C
ENST00000442157.1:c.597G>C	ENSP00000403502.1:p.Arg199=
ENST00000462980.1:n.574G>C
ENST00000491610.1:n.632G>C
NM_000884.2:c.672G>C	NP_000875.2:p.Arg224=
XM_006713128.2:c.882G>C	XP_006713191.1:p.Arg294=
XM_006713128.3:c.882G>C	XP_006713191.1:p.Arg294=
XM_017006349.1:c.807G>C	XP_016861838.1:p.Arg269=
XM_017006350.1:c.807G>C	XP_016861839.1:p.Arg269=
NM_000884.3:c.672G>C MANE Select	NP_000875.2:p.Arg224=