Canonical Allele Identifier: CA352739997

Gene: IMPDH2

Linked Data

• dbSNP Id: rs1575310132
• MyVariant Identifiers: chr3:g.49064157T>C (hg19) ; chr3:g.49026724T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49026724T>C , CM000665.2:g.49026724T>C	GRCh38
NC_000003.11:g.49064157T>C , CM000665.1:g.49064157T>C	GRCh37
NC_000003.10:g.49039161T>C	NCBI36
NG_012091.1:g.7719A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703936.1:c.2822A>G	ENSP00000515567.1:p.Asp941Gly
ENST00000703937.1:c.*1883A>G	ENSP00000515568.1:n.*1883A>G
ENST00000326739.9:c.782A>G MANE Select	ENSP00000321584.4:p.Asp261Gly
ENST00000429182.6:c.782A>G	ENSP00000393525.2:p.Asp261Gly
ENST00000442157.2:c.707A>G	ENSP00000403502.2:p.Asp236Gly
ENST00000462980.2:n.1297A>G
ENST00000472328.2:n.848A>G
ENST00000491610.2:n.742A>G
ENST00000676607.1:n.1078A>G
ENST00000676627.1:n.1512A>G
ENST00000676708.1:n.2062A>G
ENST00000676864.1:n.1931A>G
ENST00000677010.1:c.818A>G	ENSP00000503089.1:p.Asp273Gly
ENST00000677108.1:n.2688A>G
ENST00000677168.1:n.1254A>G
ENST00000677185.1:n.1345A>G
ENST00000677205.1:n.1566A>G
ENST00000677344.1:n.2056A>G
ENST00000677480.1:c.*459A>G	ENSP00000504378.1:n.*459A>G
ENST00000677519.1:n.1492A>G
ENST00000677593.1:n.1338A>G
ENST00000677740.1:n.2287A>G
ENST00000677991.1:n.1955A>G
ENST00000678001.1:n.1275A>G
ENST00000678085.1:n.1338A>G
ENST00000678177.1:n.2631A>G
ENST00000678603.1:n.1860A>G
ENST00000678724.1:c.707A>G	ENSP00000503874.1:p.Asp236Gly
ENST00000678920.1:n.940A>G
ENST00000679019.1:n.1552A>G
ENST00000679117.1:c.*597A>G	ENSP00000503240.1:n.*597A>G
ENST00000679339.1:n.1623A>G
ENST00000326739.8:c.782A>G	ENSP00000321584.4:p.Asp261Gly
ENST00000429182.5:c.576A>G
ENST00000442157.1:c.707A>G	ENSP00000403502.1:p.Asp236Gly
ENST00000462980.1:n.684A>G
ENST00000491610.1:n.742A>G
NM_000884.2:c.782A>G	NP_000875.2:p.Asp261Gly
XM_006713128.2:c.992A>G	XP_006713191.1:p.Asp331Gly
XM_006713128.3:c.992A>G	XP_006713191.1:p.Asp331Gly
XM_017006349.1:c.917A>G	XP_016861838.1:p.Asp306Gly
XM_017006350.1:c.917A>G	XP_016861839.1:p.Asp306Gly
NM_000884.3:c.782A>G MANE Select	NP_000875.2:p.Asp261Gly