Canonical Allele Identifier: CA433554497

Gene: IMPDH2

Linked Data

• MyVariant Identifiers: chr3:g.49064418A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49026985A>G , CM000665.2:g.49026985A>G	GRCh38
NC_000003.11:g.49064418A>G , CM000665.1:g.49064418A>G	GRCh37
NC_000003.10:g.49039422A>G	NCBI36
NG_012091.1:g.7458T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703936.1:c.2634T>C	ENSP00000515567.1:p.Asn878=
ENST00000703937.1:c.*1695T>C	ENSP00000515568.1:n.*1695T>C
ENST00000326739.9:c.594T>C MANE Select	ENSP00000321584.4:p.Asn198=
ENST00000429182.6:c.594T>C	ENSP00000393525.2:p.Asn198=
ENST00000442157.2:c.519T>C	ENSP00000403502.2:p.Asn173=
ENST00000462980.2:n.1109T>C
ENST00000472328.2:n.660T>C
ENST00000491610.2:n.481T>C
ENST00000676607.1:n.890T>C
ENST00000676627.1:n.1324T>C
ENST00000676708.1:n.1801T>C
ENST00000676864.1:n.1670T>C
ENST00000677010.1:c.630T>C	ENSP00000503089.1:p.Asn210=
ENST00000677108.1:n.2427T>C
ENST00000677168.1:n.1066T>C
ENST00000677185.1:n.1084T>C
ENST00000677205.1:n.1305T>C
ENST00000677344.1:n.1795T>C
ENST00000677480.1:c.*271T>C	ENSP00000504378.1:n.*271T>C
ENST00000677519.1:n.1304T>C
ENST00000677593.1:n.1077T>C
ENST00000677740.1:n.2026T>C
ENST00000677991.1:n.1767T>C
ENST00000678001.1:n.1087T>C
ENST00000678085.1:n.1077T>C
ENST00000678177.1:n.2370T>C
ENST00000678603.1:n.1672T>C
ENST00000678724.1:c.519T>C	ENSP00000503874.1:p.Asn173=
ENST00000678920.1:n.752T>C
ENST00000679019.1:n.1291T>C
ENST00000679117.1:c.*409T>C	ENSP00000503240.1:n.*409T>C
ENST00000679339.1:n.1362T>C
ENST00000326739.8:c.594T>C	ENSP00000321584.4:p.Asn198=
ENST00000429182.5:c.388T>C
ENST00000442157.1:c.519T>C	ENSP00000403502.1:p.Asn173=
ENST00000462980.1:n.496T>C
ENST00000491610.1:n.481T>C
NM_000884.2:c.594T>C	NP_000875.2:p.Asn198=
XM_006713128.2:c.804T>C	XP_006713191.1:p.Asn268=
XM_006713128.3:c.804T>C	XP_006713191.1:p.Asn268=
XM_017006349.1:c.729T>C	XP_016861838.1:p.Asn243=
XM_017006350.1:c.729T>C	XP_016861839.1:p.Asn243=
NM_000884.3:c.594T>C MANE Select	NP_000875.2:p.Asn198=