Canonical Allele Identifier: CA11569255
Gene: ARHGEF3 HGNC NCBI

Linked Data

dbSNP Id: rs13100723
gnomAD v2: 3-56798495-C-T
gnomAD v3: 3-56764467-C-T
gnomAD v4: 3-56764467-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.56764467C>T , CM000665.2:g.56764467C>T GRCh38
NC_000003.11:g.56798495C>T , CM000665.1:g.56798495C>T GRCh37
NC_000003.10:g.56773535C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000296315.8:c.204+9242G>A MANE Select ENSP00000296315.3:n.204+9242G>A
ENST00000296315.7:c.204+9242G>A ENSP00000296315.3:n.204+9242G>A
ENST00000338458.8:c.300+9242G>A ENSP00000341071.4:n.300+9242G>A
ENST00000413728.6:c.222+9242G>A ENSP00000410922.2:n.222+9242G>A
ENST00000465659.5:c.355+9242G>A
ENST00000468727.5:c.207+9242G>A ENSP00000417087.1:n.207+9242G>A
ENST00000473779.5:c.258+9242G>A ENSP00000420402.1:n.258+9242G>A
ENST00000477440.6:n.507+9242G>A
ENST00000477833.5:c.*302+9242G>A ENSP00000418984.1:n.*302+9242G>A
ENST00000481422.5:n.285+9242G>A
ENST00000495373.5:c.204+9242G>A ENSP00000417986.1:n.204+9242G>A
ENST00000496106.5:c.222+9242G>A ENSP00000420420.1:n.222+9242G>A
ENST00000497267.5:c.117+9242G>A ENSP00000418826.1:n.117+9242G>A
ENST00000498517.5:n.543+9242G>A
NM_001128615.1:c.300+9242G>A NP_001122087.1:n.300+9242G>A
NM_001128616.1:c.222+9242G>A NP_001122088.1:n.222+9242G>A
NM_001289698.1:c.222+9242G>A NP_001276627.1:n.222+9242G>A
NM_019555.2:c.204+9242G>A NP_062455.1:n.204+9242G>A
XM_005265186.3:c.300+9242G>A XP_005265243.1:n.300+9242G>A
XM_005265187.2:c.300+9242G>A XP_005265244.1:n.300+9242G>A
XM_005265188.3:c.240+9242G>A XP_005265245.1:n.240+9242G>A
XM_011533764.1:c.258+9242G>A XP_011532066.1:n.258+9242G>A
XM_011533765.1:c.207+9242G>A XP_011532067.1:n.207+9242G>A
XM_011533766.1:c.207+9242G>A XP_011532068.1:n.207+9242G>A
XM_011533767.1:c.-139+9242G>A XP_011532069.1:n.-139+9242G>A
XM_005265186.5:c.300+9242G>A XP_005265243.1:n.300+9242G>A
XM_005265187.3:c.300+9242G>A XP_005265244.1:n.300+9242G>A
XM_011533766.2:c.207+9242G>A XP_011532068.1:n.207+9242G>A
XM_017006502.1:c.240+9242G>A XP_016861991.1:n.240+9242G>A
XM_017006503.1:c.300+9242G>A XP_016861992.1:n.300+9242G>A
XM_017006504.1:c.240+9242G>A XP_016861993.1:n.240+9242G>A
XM_017006505.1:c.204+9242G>A XP_016861994.1:n.204+9242G>A
XM_017006506.2:c.222+9242G>A XP_016861995.1:n.222+9242G>A
XM_024453546.1:c.240+9242G>A XP_024309314.1:n.240+9242G>A
XM_024453547.1:c.240+9242G>A XP_024309315.1:n.240+9242G>A
NM_001128615.2:c.300+9242G>A NP_001122087.1:n.300+9242G>A
NM_001128616.2:c.222+9242G>A NP_001122088.1:n.222+9242G>A
NM_001289698.2:c.222+9242G>A NP_001276627.1:n.222+9242G>A
NM_001377407.1:c.300+9242G>A NP_001364336.1:n.300+9242G>A
NM_001377408.1:c.240+9242G>A NP_001364337.1:n.240+9242G>A
NM_001377409.1:c.240+9242G>A NP_001364338.1:n.240+9242G>A
NM_001377410.1:c.240+9242G>A NP_001364339.1:n.240+9242G>A
NM_001377411.1:c.207+9242G>A NP_001364340.1:n.207+9242G>A
NM_001377412.1:c.207+9242G>A NP_001364341.1:n.207+9242G>A
NM_001377413.1:c.222+9242G>A NP_001364342.1:n.222+9242G>A
NM_001377414.1:c.204+9242G>A NP_001364343.1:n.204+9242G>A
NM_001377415.1:c.204+9242G>A NP_001364344.1:n.204+9242G>A
NM_019555.3:c.204+9242G>A MANE Select NP_062455.1:n.204+9242G>A