Canonical Allele Identifier: CA433629706

Gene: IMPDH2

Linked Data

• MyVariant Identifiers: chr3:g.49064300A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49026867A>G , CM000665.2:g.49026867A>G	GRCh38
NC_000003.11:g.49064300A>G , CM000665.1:g.49064300A>G	GRCh37
NC_000003.10:g.49039304A>G	NCBI36
NG_012091.1:g.7576T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703936.1:c.2679T>C	ENSP00000515567.1:p.Asn893=
ENST00000703937.1:c.*1740T>C	ENSP00000515568.1:n.*1740T>C
ENST00000326739.9:c.639T>C MANE Select	ENSP00000321584.4:p.Asn213=
ENST00000429182.6:c.639T>C	ENSP00000393525.2:p.Asn213=
ENST00000442157.2:c.564T>C	ENSP00000403502.2:p.Asn188=
ENST00000462980.2:n.1154T>C
ENST00000472328.2:n.705T>C
ENST00000491610.2:n.599T>C
ENST00000676607.1:n.935T>C
ENST00000676627.1:n.1369T>C
ENST00000676708.1:n.1919T>C
ENST00000676864.1:n.1788T>C
ENST00000677010.1:c.675T>C	ENSP00000503089.1:p.Asn225=
ENST00000677108.1:n.2545T>C
ENST00000677168.1:n.1111T>C
ENST00000677185.1:n.1202T>C
ENST00000677205.1:n.1423T>C
ENST00000677344.1:n.1913T>C
ENST00000677480.1:c.*316T>C	ENSP00000504378.1:n.*316T>C
ENST00000677519.1:n.1349T>C
ENST00000677593.1:n.1195T>C
ENST00000677740.1:n.2144T>C
ENST00000677991.1:n.1812T>C
ENST00000678001.1:n.1132T>C
ENST00000678085.1:n.1195T>C
ENST00000678177.1:n.2488T>C
ENST00000678603.1:n.1717T>C
ENST00000678724.1:c.564T>C	ENSP00000503874.1:p.Asn188=
ENST00000678920.1:n.797T>C
ENST00000679019.1:n.1409T>C
ENST00000679117.1:c.*454T>C	ENSP00000503240.1:n.*454T>C
ENST00000679339.1:n.1480T>C
ENST00000326739.8:c.639T>C	ENSP00000321584.4:p.Asn213=
ENST00000429182.5:c.433T>C
ENST00000442157.1:c.564T>C	ENSP00000403502.1:p.Asn188=
ENST00000462980.1:n.541T>C
ENST00000491610.1:n.599T>C
NM_000884.2:c.639T>C	NP_000875.2:p.Asn213=
XM_006713128.2:c.849T>C	XP_006713191.1:p.Asn283=
XM_006713128.3:c.849T>C	XP_006713191.1:p.Asn283=
XM_017006349.1:c.774T>C	XP_016861838.1:p.Asn258=
XM_017006350.1:c.774T>C	XP_016861839.1:p.Asn258=
NM_000884.3:c.639T>C MANE Select	NP_000875.2:p.Asn213=