Canonical Allele Identifier: CA352741595

Gene: IMPDH2

Linked Data

• MyVariant Identifiers: chr3:g.49064405G>C (hg19) ; chr3:g.49026972G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49026972G>C , CM000665.2:g.49026972G>C	GRCh38
NC_000003.11:g.49064405G>C , CM000665.1:g.49064405G>C	GRCh37
NC_000003.10:g.49039409G>C	NCBI36
NG_012091.1:g.7471C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703936.1:c.2647C>G	ENSP00000515567.1:p.Arg883Gly
ENST00000703937.1:c.*1708C>G	ENSP00000515568.1:n.*1708C>G
ENST00000326739.9:c.607C>G MANE Select	ENSP00000321584.4:p.Arg203Gly
ENST00000429182.6:c.607C>G	ENSP00000393525.2:p.Arg203Gly
ENST00000442157.2:c.532C>G	ENSP00000403502.2:p.Arg178Gly
ENST00000462980.2:n.1122C>G
ENST00000472328.2:n.673C>G
ENST00000491610.2:n.494C>G
ENST00000676607.1:n.903C>G
ENST00000676627.1:n.1337C>G
ENST00000676708.1:n.1814C>G
ENST00000676864.1:n.1683C>G
ENST00000677010.1:c.643C>G	ENSP00000503089.1:p.Arg215Gly
ENST00000677108.1:n.2440C>G
ENST00000677168.1:n.1079C>G
ENST00000677185.1:n.1097C>G
ENST00000677205.1:n.1318C>G
ENST00000677344.1:n.1808C>G
ENST00000677480.1:c.*284C>G	ENSP00000504378.1:n.*284C>G
ENST00000677519.1:n.1317C>G
ENST00000677593.1:n.1090C>G
ENST00000677740.1:n.2039C>G
ENST00000677991.1:n.1780C>G
ENST00000678001.1:n.1100C>G
ENST00000678085.1:n.1090C>G
ENST00000678177.1:n.2383C>G
ENST00000678603.1:n.1685C>G
ENST00000678724.1:c.532C>G	ENSP00000503874.1:p.Arg178Gly
ENST00000678920.1:n.765C>G
ENST00000679019.1:n.1304C>G
ENST00000679117.1:c.*422C>G	ENSP00000503240.1:n.*422C>G
ENST00000679339.1:n.1375C>G
ENST00000326739.8:c.607C>G	ENSP00000321584.4:p.Arg203Gly
ENST00000429182.5:c.401C>G
ENST00000442157.1:c.532C>G	ENSP00000403502.1:p.Arg178Gly
ENST00000462980.1:n.509C>G
ENST00000491610.1:n.494C>G
NM_000884.2:c.607C>G	NP_000875.2:p.Arg203Gly
XM_006713128.2:c.817C>G	XP_006713191.1:p.Arg273Gly
XM_006713128.3:c.817C>G	XP_006713191.1:p.Arg273Gly
XM_017006349.1:c.742C>G	XP_016861838.1:p.Arg248Gly
XM_017006350.1:c.742C>G	XP_016861839.1:p.Arg248Gly
NM_000884.3:c.607C>G MANE Select	NP_000875.2:p.Arg203Gly