Canonical Allele Identifier: CA352740512

Gene: IMPDH2

Linked Data

• MyVariant Identifiers: chr3:g.49064230A>T (hg19) ; chr3:g.49026797A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49026797A>T , CM000665.2:g.49026797A>T	GRCh38
NC_000003.11:g.49064230A>T , CM000665.1:g.49064230A>T	GRCh37
NC_000003.10:g.49039234A>T	NCBI36
NG_012091.1:g.7646T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703936.1:c.2749T>A	ENSP00000515567.1:p.Ser917Thr
ENST00000703937.1:c.*1810T>A	ENSP00000515568.1:n.*1810T>A
ENST00000326739.9:c.709T>A MANE Select	ENSP00000321584.4:p.Ser237Thr
ENST00000429182.6:c.709T>A	ENSP00000393525.2:p.Ser237Thr
ENST00000442157.2:c.634T>A	ENSP00000403502.2:p.Ser212Thr
ENST00000462980.2:n.1224T>A
ENST00000472328.2:n.775T>A
ENST00000491610.2:n.669T>A
ENST00000676607.1:n.1005T>A
ENST00000676627.1:n.1439T>A
ENST00000676708.1:n.1989T>A
ENST00000676864.1:n.1858T>A
ENST00000677010.1:c.745T>A	ENSP00000503089.1:p.Ser249Thr
ENST00000677108.1:n.2615T>A
ENST00000677168.1:n.1181T>A
ENST00000677185.1:n.1272T>A
ENST00000677205.1:n.1493T>A
ENST00000677344.1:n.1983T>A
ENST00000677480.1:c.*386T>A	ENSP00000504378.1:n.*386T>A
ENST00000677519.1:n.1419T>A
ENST00000677593.1:n.1265T>A
ENST00000677740.1:n.2214T>A
ENST00000677991.1:n.1882T>A
ENST00000678001.1:n.1202T>A
ENST00000678085.1:n.1265T>A
ENST00000678177.1:n.2558T>A
ENST00000678603.1:n.1787T>A
ENST00000678724.1:c.634T>A	ENSP00000503874.1:p.Ser212Thr
ENST00000678920.1:n.867T>A
ENST00000679019.1:n.1479T>A
ENST00000679117.1:c.*524T>A	ENSP00000503240.1:n.*524T>A
ENST00000679339.1:n.1550T>A
ENST00000326739.8:c.709T>A	ENSP00000321584.4:p.Ser237Thr
ENST00000429182.5:c.503T>A
ENST00000442157.1:c.634T>A	ENSP00000403502.1:p.Ser212Thr
ENST00000462980.1:n.611T>A
ENST00000491610.1:n.669T>A
NM_000884.2:c.709T>A	NP_000875.2:p.Ser237Thr
XM_006713128.2:c.919T>A	XP_006713191.1:p.Ser307Thr
XM_006713128.3:c.919T>A	XP_006713191.1:p.Ser307Thr
XM_017006349.1:c.844T>A	XP_016861838.1:p.Ser282Thr
XM_017006350.1:c.844T>A	XP_016861839.1:p.Ser282Thr
NM_000884.3:c.709T>A MANE Select	NP_000875.2:p.Ser237Thr