Canonical Allele Identifier: CA433629708

Gene: IMPDH2

Linked Data

• MyVariant Identifiers: chr3:g.49064303T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49026870T>A , CM000665.2:g.49026870T>A	GRCh38
NC_000003.11:g.49064303T>A , CM000665.1:g.49064303T>A	GRCh37
NC_000003.10:g.49039307T>A	NCBI36
NG_012091.1:g.7573A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703936.1:c.2676A>T	ENSP00000515567.1:p.Val892=
ENST00000703937.1:c.*1737A>T	ENSP00000515568.1:n.*1737A>T
ENST00000326739.9:c.636A>T MANE Select	ENSP00000321584.4:p.Val212=
ENST00000429182.6:c.636A>T	ENSP00000393525.2:p.Val212=
ENST00000442157.2:c.561A>T	ENSP00000403502.2:p.Val187=
ENST00000462980.2:n.1151A>T
ENST00000472328.2:n.702A>T
ENST00000491610.2:n.596A>T
ENST00000676607.1:n.932A>T
ENST00000676627.1:n.1366A>T
ENST00000676708.1:n.1916A>T
ENST00000676864.1:n.1785A>T
ENST00000677010.1:c.672A>T	ENSP00000503089.1:p.Val224=
ENST00000677108.1:n.2542A>T
ENST00000677168.1:n.1108A>T
ENST00000677185.1:n.1199A>T
ENST00000677205.1:n.1420A>T
ENST00000677344.1:n.1910A>T
ENST00000677480.1:c.*313A>T	ENSP00000504378.1:n.*313A>T
ENST00000677519.1:n.1346A>T
ENST00000677593.1:n.1192A>T
ENST00000677740.1:n.2141A>T
ENST00000677991.1:n.1809A>T
ENST00000678001.1:n.1129A>T
ENST00000678085.1:n.1192A>T
ENST00000678177.1:n.2485A>T
ENST00000678603.1:n.1714A>T
ENST00000678724.1:c.561A>T	ENSP00000503874.1:p.Val187=
ENST00000678920.1:n.794A>T
ENST00000679019.1:n.1406A>T
ENST00000679117.1:c.*451A>T	ENSP00000503240.1:n.*451A>T
ENST00000679339.1:n.1477A>T
ENST00000326739.8:c.636A>T	ENSP00000321584.4:p.Val212=
ENST00000429182.5:c.430A>T
ENST00000442157.1:c.561A>T	ENSP00000403502.1:p.Val187=
ENST00000462980.1:n.538A>T
ENST00000491610.1:n.596A>T
NM_000884.2:c.636A>T	NP_000875.2:p.Val212=
XM_006713128.2:c.846A>T	XP_006713191.1:p.Val282=
XM_006713128.3:c.846A>T	XP_006713191.1:p.Val282=
XM_017006349.1:c.771A>T	XP_016861838.1:p.Val257=
XM_017006350.1:c.771A>T	XP_016861839.1:p.Val257=
NM_000884.3:c.636A>T MANE Select	NP_000875.2:p.Val212=