Canonical Allele Identifier: CA9136892
Gene: ARHGEF18 HGNC NCBI

Linked Data

ClinVar Variation Id: 934092
ClinVar RCV Id: RCV001202427
dbSNP Id: rs143766225
gnomAD v2: 19-7527121-G-A
gnomAD v3: 19-7462235-G-A
gnomAD v4: 19-7462235-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7462235G>A , CM000681.2:g.7462235G>A GRCh38
NC_000019.9:g.7527121G>A , CM000681.1:g.7527121G>A GRCh37
NC_000019.8:g.7433121G>A NCBI36
NG_047135.1:g.118325G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000319670.14:c.1498G>A ENSP00000319200.8:p.Gly500Ser
ENST00000359920.11:c.1810G>A ENSP00000352995.5:p.Gly604Ser
ENST00000594665.2:c.1498G>A ENSP00000470729.2:p.Gly500Ser
ENST00000617428.4:c.1498G>A ENSP00000482647.4:p.Gly500Ser
ENST00000668164.2:c.2536G>A MANE Select ENSP00000499655.2:p.Gly846Ser
ENST00000319670.13:c.1498G>A ENSP00000319200.7:p.Gly500Ser
ENST00000359920.10:c.1972G>A ENSP00000352995.4:p.Gly658Ser
ENST00000594665.1:c.905G>A
ENST00000617428.2:c.1772G>A
NM_001130955.1:c.1972G>A NP_001124427.1:p.Gly658Ser
NM_015318.3:c.1498G>A NP_056133.2:p.Gly500Ser
XM_005272464.3:c.2731G>A XP_005272521.1:p.Gly911Ser
XM_006722705.2:c.2536G>A XP_006722768.1:p.Gly846Ser
XM_006722706.2:c.2536G>A XP_006722769.1:p.Gly846Ser
XM_006722708.2:c.1498G>A XP_006722771.1:p.Gly500Ser
XM_006722709.2:c.1498G>A XP_006722772.1:p.Gly500Ser
XM_011527835.1:c.2731G>A XP_011526137.1:p.Gly911Ser
XM_011527836.1:c.2731G>A XP_011526138.1:p.Gly911Ser
XM_011527837.1:c.2731G>A XP_011526139.1:p.Gly911Ser
XM_011527838.1:c.2536G>A XP_011526140.1:p.Gly846Ser
XM_011527839.1:c.2488G>A XP_011526141.1:p.Gly830Ser
XM_011527840.1:c.1498G>A XP_011526142.1:p.Gly500Ser
XM_011527841.1:c.2731G>A XP_011526143.1:p.Gly911Ser
XM_005272464.4:c.2731G>A XP_005272521.1:p.Gly911Ser
XM_006722705.3:c.2536G>A XP_006722768.1:p.Gly846Ser
XM_006722706.3:c.2536G>A XP_006722769.1:p.Gly846Ser
XM_011527835.2:c.2731G>A XP_011526137.1:p.Gly911Ser
XM_011527836.2:c.2731G>A XP_011526138.1:p.Gly911Ser
XM_011527837.2:c.2731G>A XP_011526139.1:p.Gly911Ser
XM_011527838.3:c.2536G>A XP_011526140.1:p.Gly846Ser
XM_011527839.2:c.2488G>A XP_011526141.1:p.Gly830Ser
XM_011527840.2:c.1498G>A XP_011526142.1:p.Gly500Ser
XM_011527841.2:c.2731G>A XP_011526143.1:p.Gly911Ser
NM_001130955.2:c.1810G>A NP_001124427.2:p.Gly604Ser
NM_001367823.1:c.2536G>A MANE Select NP_001354752.1:p.Gly846Ser
NM_001367824.1:c.1498G>A NP_001354753.1:p.Gly500Ser
NM_015318.4:c.1498G>A NP_056133.2:p.Gly500Ser