Canonical Allele Identifier: CA352741184

Gene: IMPDH2

Linked Data

• MyVariant Identifiers: chr3:g.49064308T>C (hg19) ; chr3:g.49026875T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49026875T>C , CM000665.2:g.49026875T>C	GRCh38
NC_000003.11:g.49064308T>C , CM000665.1:g.49064308T>C	GRCh37
NC_000003.10:g.49039312T>C	NCBI36
NG_012091.1:g.7568A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703936.1:c.2671A>G	ENSP00000515567.1:p.Ile891Val
ENST00000703937.1:c.*1732A>G	ENSP00000515568.1:n.*1732A>G
ENST00000326739.9:c.631A>G MANE Select	ENSP00000321584.4:p.Ile211Val
ENST00000429182.6:c.631A>G	ENSP00000393525.2:p.Ile211Val
ENST00000442157.2:c.556A>G	ENSP00000403502.2:p.Ile186Val
ENST00000462980.2:n.1146A>G
ENST00000472328.2:n.697A>G
ENST00000491610.2:n.591A>G
ENST00000676607.1:n.927A>G
ENST00000676627.1:n.1361A>G
ENST00000676708.1:n.1911A>G
ENST00000676864.1:n.1780A>G
ENST00000677010.1:c.667A>G	ENSP00000503089.1:p.Ile223Val
ENST00000677108.1:n.2537A>G
ENST00000677168.1:n.1103A>G
ENST00000677185.1:n.1194A>G
ENST00000677205.1:n.1415A>G
ENST00000677344.1:n.1905A>G
ENST00000677480.1:c.*308A>G	ENSP00000504378.1:n.*308A>G
ENST00000677519.1:n.1341A>G
ENST00000677593.1:n.1187A>G
ENST00000677740.1:n.2136A>G
ENST00000677991.1:n.1804A>G
ENST00000678001.1:n.1124A>G
ENST00000678085.1:n.1187A>G
ENST00000678177.1:n.2480A>G
ENST00000678603.1:n.1709A>G
ENST00000678724.1:c.556A>G	ENSP00000503874.1:p.Ile186Val
ENST00000678920.1:n.789A>G
ENST00000679019.1:n.1401A>G
ENST00000679117.1:c.*446A>G	ENSP00000503240.1:n.*446A>G
ENST00000679339.1:n.1472A>G
ENST00000326739.8:c.631A>G	ENSP00000321584.4:p.Ile211Val
ENST00000429182.5:c.425A>G
ENST00000442157.1:c.556A>G	ENSP00000403502.1:p.Ile186Val
ENST00000462980.1:n.533A>G
ENST00000491610.1:n.591A>G
NM_000884.2:c.631A>G	NP_000875.2:p.Ile211Val
XM_006713128.2:c.841A>G	XP_006713191.1:p.Ile281Val
XM_006713128.3:c.841A>G	XP_006713191.1:p.Ile281Val
XM_017006349.1:c.766A>G	XP_016861838.1:p.Ile256Val
XM_017006350.1:c.766A>G	XP_016861839.1:p.Ile256Val
NM_000884.3:c.631A>G MANE Select	NP_000875.2:p.Ile211Val