Canonical Allele Identifier: CA8169272
Gene: RFWD3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1327953
dbSNP Id: rs4888262

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.74636560C>T , CM000678.2:g.74636560C>T GRCh38
NC_000016.9:g.74670458C>T , CM000678.1:g.74670458C>T GRCh37
NC_000016.8:g.73227959C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000361070.9:c.1212G>A MANE Select ENSP00000354361.4:p.Thr404=
ENST00000361070.8:c.1212G>A ENSP00000354361.4:p.Thr404=
ENST00000571750.5:c.1212G>A ENSP00000460049.1:p.Thr404=
NM_018124.3:c.1212G>A NP_060594.3:p.Thr404=
XM_005256021.3:c.1212G>A XP_005256078.1:p.Thr404=
XM_005256022.3:c.1212G>A XP_005256079.1:p.Thr404=
XM_006721228.2:c.1212G>A XP_006721291.1:p.Thr404=
XM_011523191.1:c.1212G>A XP_011521493.1:p.Thr404=
XM_005256021.4:c.1212G>A XP_005256078.1:p.Thr404=
XM_005256022.4:c.1212G>A XP_005256079.1:p.Thr404=
XM_006721228.3:c.1212G>A XP_006721291.1:p.Thr404=
XM_011523191.3:c.1212G>A XP_011521493.1:p.Thr404=
XM_017023391.1:c.1212G>A XP_016878880.1:p.Thr404=
XM_017023392.1:c.1212G>A XP_016878881.1:p.Thr404=
NM_018124.4:c.1212G>A MANE Select NP_060594.3:p.Thr404=
NM_001370534.1:c.1212G>A NP_001357463.1:p.Thr404=
NM_001370535.1:c.1212G>A NP_001357464.1:p.Thr404=
NM_001370536.1:c.1212G>A NP_001357465.1:p.Thr404=
NM_001370537.1:c.378G>A NP_001357466.1:p.Thr126=
NM_001370539.1:c.378G>A NP_001357468.1:p.Thr126=
NM_001370540.1:c.378G>A NP_001357469.1:p.Thr126=
NM_001370542.1:c.378G>A NP_001357471.1:p.Thr126=
NM_001370543.1:c.378G>A NP_001357472.1:p.Thr126=