Canonical Allele Identifier: CA907788519

Gene: IMPDH2

Linked Data

• dbSNP Id: rs1369604037
• MyVariant Identifiers: chr3:g.49064367G>A (hg19) ; chr3:g.49026934G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49026934G>A , CM000665.2:g.49026934G>A	GRCh38
NC_000003.11:g.49064367G>A , CM000665.1:g.49064367G>A	GRCh37
NC_000003.10:g.49039371G>A	NCBI36
NG_012091.1:g.7509C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703936.1:c.2659+26C>T	ENSP00000515567.1:n.2659+26C>T
ENST00000703937.1:c.*1720+26C>T	ENSP00000515568.1:n.*1720+26C>T
ENST00000326739.9:c.619+26C>T MANE Select	ENSP00000321584.4:n.619+26C>T
ENST00000429182.6:c.619+26C>T	ENSP00000393525.2:n.619+26C>T
ENST00000442157.2:c.544+26C>T	ENSP00000403502.2:n.544+26C>T
ENST00000462980.2:n.1134+26C>T
ENST00000472328.2:n.685+26C>T
ENST00000491610.2:n.532C>T
ENST00000676607.1:n.915+26C>T
ENST00000676627.1:n.1349+26C>T
ENST00000676708.1:n.1852C>T
ENST00000676864.1:n.1721C>T
ENST00000677010.1:c.655+26C>T	ENSP00000503089.1:n.655+26C>T
ENST00000677108.1:n.2478C>T
ENST00000677168.1:n.1091+26C>T
ENST00000677185.1:n.1135C>T
ENST00000677205.1:n.1356C>T
ENST00000677344.1:n.1846C>T
ENST00000677480.1:c.*296+26C>T	ENSP00000504378.1:n.*296+26C>T
ENST00000677519.1:n.1329+26C>T
ENST00000677593.1:n.1128C>T
ENST00000677740.1:n.2077C>T
ENST00000677991.1:n.1792+26C>T
ENST00000678001.1:n.1112+26C>T
ENST00000678085.1:n.1128C>T
ENST00000678177.1:n.2421C>T
ENST00000678603.1:n.1697+26C>T
ENST00000678724.1:c.544+26C>T	ENSP00000503874.1:n.544+26C>T
ENST00000678920.1:n.777+26C>T
ENST00000679019.1:n.1342C>T
ENST00000679117.1:c.*434+26C>T	ENSP00000503240.1:n.*434+26C>T
ENST00000679339.1:n.1413C>T
ENST00000326739.8:c.619+26C>T	ENSP00000321584.4:n.619+26C>T
ENST00000429182.5:c.413+26C>T
ENST00000442157.1:c.544+26C>T	ENSP00000403502.1:n.544+26C>T
ENST00000462980.1:n.521+26C>T
ENST00000491610.1:n.532C>T
NM_000884.2:c.619+26C>T	NP_000875.2:n.619+26C>T
XM_006713128.2:c.829+26C>T	XP_006713191.1:n.829+26C>T
XM_006713128.3:c.829+26C>T	XP_006713191.1:n.829+26C>T
XM_017006349.1:c.754+26C>T	XP_016861838.1:n.754+26C>T
XM_017006350.1:c.754+26C>T	XP_016861839.1:n.754+26C>T
NM_000884.3:c.619+26C>T MANE Select	NP_000875.2:n.619+26C>T