Canonical Allele Identifier: CA352741133

Gene: IMPDH2

Linked Data

• MyVariant Identifiers: chr3:g.49064304A>C (hg19) ; chr3:g.49026871A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49026871A>C , CM000665.2:g.49026871A>C	GRCh38
NC_000003.11:g.49064304A>C , CM000665.1:g.49064304A>C	GRCh37
NC_000003.10:g.49039308A>C	NCBI36
NG_012091.1:g.7572T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703936.1:c.2675T>G	ENSP00000515567.1:p.Val892Gly
ENST00000703937.1:c.*1736T>G	ENSP00000515568.1:n.*1736T>G
ENST00000326739.9:c.635T>G MANE Select	ENSP00000321584.4:p.Val212Gly
ENST00000429182.6:c.635T>G	ENSP00000393525.2:p.Val212Gly
ENST00000442157.2:c.560T>G	ENSP00000403502.2:p.Val187Gly
ENST00000462980.2:n.1150T>G
ENST00000472328.2:n.701T>G
ENST00000491610.2:n.595T>G
ENST00000676607.1:n.931T>G
ENST00000676627.1:n.1365T>G
ENST00000676708.1:n.1915T>G
ENST00000676864.1:n.1784T>G
ENST00000677010.1:c.671T>G	ENSP00000503089.1:p.Val224Gly
ENST00000677108.1:n.2541T>G
ENST00000677168.1:n.1107T>G
ENST00000677185.1:n.1198T>G
ENST00000677205.1:n.1419T>G
ENST00000677344.1:n.1909T>G
ENST00000677480.1:c.*312T>G	ENSP00000504378.1:n.*312T>G
ENST00000677519.1:n.1345T>G
ENST00000677593.1:n.1191T>G
ENST00000677740.1:n.2140T>G
ENST00000677991.1:n.1808T>G
ENST00000678001.1:n.1128T>G
ENST00000678085.1:n.1191T>G
ENST00000678177.1:n.2484T>G
ENST00000678603.1:n.1713T>G
ENST00000678724.1:c.560T>G	ENSP00000503874.1:p.Val187Gly
ENST00000678920.1:n.793T>G
ENST00000679019.1:n.1405T>G
ENST00000679117.1:c.*450T>G	ENSP00000503240.1:n.*450T>G
ENST00000679339.1:n.1476T>G
ENST00000326739.8:c.635T>G	ENSP00000321584.4:p.Val212Gly
ENST00000429182.5:c.429T>G
ENST00000442157.1:c.560T>G	ENSP00000403502.1:p.Val187Gly
ENST00000462980.1:n.537T>G
ENST00000491610.1:n.595T>G
NM_000884.2:c.635T>G	NP_000875.2:p.Val212Gly
XM_006713128.2:c.845T>G	XP_006713191.1:p.Val282Gly
XM_006713128.3:c.845T>G	XP_006713191.1:p.Val282Gly
XM_017006349.1:c.770T>G	XP_016861838.1:p.Val257Gly
XM_017006350.1:c.770T>G	XP_016861839.1:p.Val257Gly
NM_000884.3:c.635T>G MANE Select	NP_000875.2:p.Val212Gly