Canonical Allele Identifier: CA352739881

Gene: IMPDH2

Linked Data

• dbSNP Id: rs886766695
• MyVariant Identifiers: chr3:g.49064139C>G (hg19) ; chr3:g.49026706C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49026706C>G , CM000665.2:g.49026706C>G	GRCh38
NC_000003.11:g.49064139C>G , CM000665.1:g.49064139C>G	GRCh37
NC_000003.10:g.49039143C>G	NCBI36
NG_012091.1:g.7737G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703936.1:c.2840G>C	ENSP00000515567.1:p.Gly947Ala
ENST00000703937.1:c.*1901G>C	ENSP00000515568.1:n.*1901G>C
ENST00000326739.9:c.800G>C MANE Select	ENSP00000321584.4:p.Gly267Ala
ENST00000429182.6:c.800G>C	ENSP00000393525.2:p.Gly267Ala
ENST00000442157.2:c.725G>C	ENSP00000403502.2:p.Gly242Ala
ENST00000462980.2:n.1315G>C
ENST00000472328.2:n.866G>C
ENST00000491610.2:n.760G>C
ENST00000676607.1:n.1096G>C
ENST00000676627.1:n.1530G>C
ENST00000676708.1:n.2080G>C
ENST00000676864.1:n.1949G>C
ENST00000677010.1:c.836G>C	ENSP00000503089.1:p.Gly279Ala
ENST00000677108.1:n.2706G>C
ENST00000677168.1:n.1272G>C
ENST00000677185.1:n.1363G>C
ENST00000677205.1:n.1584G>C
ENST00000677344.1:n.2074G>C
ENST00000677480.1:c.*477G>C	ENSP00000504378.1:n.*477G>C
ENST00000677519.1:n.1510G>C
ENST00000677593.1:n.1356G>C
ENST00000677740.1:n.2305G>C
ENST00000677991.1:n.1973G>C
ENST00000678001.1:n.1293G>C
ENST00000678085.1:n.1356G>C
ENST00000678177.1:n.2649G>C
ENST00000678603.1:n.1878G>C
ENST00000678724.1:c.725G>C	ENSP00000503874.1:p.Gly242Ala
ENST00000678920.1:n.958G>C
ENST00000679019.1:n.1570G>C
ENST00000679117.1:c.*615G>C	ENSP00000503240.1:n.*615G>C
ENST00000679339.1:n.1641G>C
ENST00000326739.8:c.800G>C	ENSP00000321584.4:p.Gly267Ala
ENST00000429182.5:c.594G>C
ENST00000442157.1:c.725G>C	ENSP00000403502.1:p.Gly242Ala
ENST00000462980.1:n.702G>C
ENST00000491610.1:n.760G>C
NM_000884.2:c.800G>C	NP_000875.2:p.Gly267Ala
XM_006713128.2:c.1010G>C	XP_006713191.1:p.Gly337Ala
XM_006713128.3:c.1010G>C	XP_006713191.1:p.Gly337Ala
XM_017006349.1:c.935G>C	XP_016861838.1:p.Gly312Ala
XM_017006350.1:c.935G>C	XP_016861839.1:p.Gly312Ala
NM_000884.3:c.800G>C MANE Select	NP_000875.2:p.Gly267Ala