Canonical Allele Identifier: CA496543423
Gene: RFWD3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.74670440A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.74636542A>G , CM000678.2:g.74636542A>G GRCh38
NC_000016.9:g.74670440A>G , CM000678.1:g.74670440A>G GRCh37
NC_000016.8:g.73227941A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000361070.9:c.1230T>C MANE Select ENSP00000354361.4:p.Asn410=
ENST00000361070.8:c.1230T>C ENSP00000354361.4:p.Asn410=
ENST00000571750.5:c.1230T>C ENSP00000460049.1:p.Asn410=
NM_018124.3:c.1230T>C NP_060594.3:p.Asn410=
XM_005256021.3:c.1230T>C XP_005256078.1:p.Asn410=
XM_005256022.3:c.1230T>C XP_005256079.1:p.Asn410=
XM_006721228.2:c.1230T>C XP_006721291.1:p.Asn410=
XM_011523191.1:c.1230T>C XP_011521493.1:p.Asn410=
XM_005256021.4:c.1230T>C XP_005256078.1:p.Asn410=
XM_005256022.4:c.1230T>C XP_005256079.1:p.Asn410=
XM_006721228.3:c.1230T>C XP_006721291.1:p.Asn410=
XM_011523191.3:c.1230T>C XP_011521493.1:p.Asn410=
XM_017023391.1:c.1230T>C XP_016878880.1:p.Asn410=
XM_017023392.1:c.1230T>C XP_016878881.1:p.Asn410=
NM_018124.4:c.1230T>C MANE Select NP_060594.3:p.Asn410=
NM_001370534.1:c.1230T>C NP_001357463.1:p.Asn410=
NM_001370535.1:c.1230T>C NP_001357464.1:p.Asn410=
NM_001370536.1:c.1230T>C NP_001357465.1:p.Asn410=
NM_001370537.1:c.396T>C NP_001357466.1:p.Asn132=
NM_001370539.1:c.396T>C NP_001357468.1:p.Asn132=
NM_001370540.1:c.396T>C NP_001357469.1:p.Asn132=
NM_001370542.1:c.396T>C NP_001357471.1:p.Asn132=
NM_001370543.1:c.396T>C NP_001357472.1:p.Asn132=