Canonical Allele Identifier: CA433629498

Gene: IMPDH2

Linked Data

• MyVariant Identifiers: chr3:g.49064138A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49026705A>C , CM000665.2:g.49026705A>C	GRCh38
NC_000003.11:g.49064138A>C , CM000665.1:g.49064138A>C	GRCh37
NC_000003.10:g.49039142A>C	NCBI36
NG_012091.1:g.7738T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703936.1:c.2841T>G	ENSP00000515567.1:p.Gly947=
ENST00000703937.1:c.*1902T>G	ENSP00000515568.1:n.*1902T>G
ENST00000326739.9:c.801T>G MANE Select	ENSP00000321584.4:p.Gly267=
ENST00000429182.6:c.801T>G	ENSP00000393525.2:p.Gly267=
ENST00000442157.2:c.726T>G	ENSP00000403502.2:p.Gly242=
ENST00000462980.2:n.1316T>G
ENST00000472328.2:n.867T>G
ENST00000491610.2:n.761T>G
ENST00000676607.1:n.1097T>G
ENST00000676627.1:n.1531T>G
ENST00000676708.1:n.2081T>G
ENST00000676864.1:n.1950T>G
ENST00000677010.1:c.837T>G	ENSP00000503089.1:p.Gly279=
ENST00000677108.1:n.2707T>G
ENST00000677168.1:n.1273T>G
ENST00000677185.1:n.1364T>G
ENST00000677205.1:n.1585T>G
ENST00000677344.1:n.2075T>G
ENST00000677480.1:c.*478T>G	ENSP00000504378.1:n.*478T>G
ENST00000677519.1:n.1511T>G
ENST00000677593.1:n.1357T>G
ENST00000677740.1:n.2306T>G
ENST00000677991.1:n.1974T>G
ENST00000678001.1:n.1294T>G
ENST00000678085.1:n.1357T>G
ENST00000678177.1:n.2650T>G
ENST00000678603.1:n.1879T>G
ENST00000678724.1:c.726T>G	ENSP00000503874.1:p.Gly242=
ENST00000678920.1:n.959T>G
ENST00000679019.1:n.1571T>G
ENST00000679117.1:c.*616T>G	ENSP00000503240.1:n.*616T>G
ENST00000679339.1:n.1642T>G
ENST00000326739.8:c.801T>G	ENSP00000321584.4:p.Gly267=
ENST00000429182.5:c.595T>G
ENST00000442157.1:c.726T>G	ENSP00000403502.1:p.Gly242=
ENST00000462980.1:n.703T>G
ENST00000491610.1:n.761T>G
NM_000884.2:c.801T>G	NP_000875.2:p.Gly267=
XM_006713128.2:c.1011T>G	XP_006713191.1:p.Gly337=
XM_006713128.3:c.1011T>G	XP_006713191.1:p.Gly337=
XM_017006349.1:c.936T>G	XP_016861838.1:p.Gly312=
XM_017006350.1:c.936T>G	XP_016861839.1:p.Gly312=
NM_000884.3:c.801T>G MANE Select	NP_000875.2:p.Gly267=