Canonical Allele Identifier: CA210355
Gene: FTO HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 217824
ClinVar RCV Id: RCV000201907
dbSNP Id: rs1421085

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.53767042T>C , CM000678.2:g.53767042T>C GRCh38
NC_000016.9:g.53800954T>C , CM000678.1:g.53800954T>C GRCh37
NC_000016.8:g.52358455T>C NCBI36
NG_012969.1:g.68080T>C

Transcript Alleles

HGVS Amino-acid change
NM_001080432.2:c.46-43098T>C VV NP_001073901.1:p.=
XM_011523313.1:c.46-43098T>C XP_011521615.1:p.=
XM_011523314.1:c.46-43098T>C XP_011521616.1:p.=
XM_011523315.1:c.46-43098T>C XP_011521617.1:p.=
XM_011523316.1:c.46-43098T>C XP_011521618.1:p.=
NM_001363891.1:c.46-43098T>C VV NP_001350820.1:p.=
NM_001363894.1:c.46-43098T>C VV NP_001350823.1:p.=
NM_001363896.1:c.46-43098T>C VV NP_001350825.1:p.=
NM_001363897.1:c.46-58822T>C VV NP_001350826.1:p.=
NM_001363898.1:c.46-43098T>C VV NP_001350827.1:p.=
NM_001363899.1:c.46-43098T>C VV NP_001350828.1:p.=
NM_001363900.1:c.46-43098T>C VV NP_001350829.1:p.=
NM_001363901.1:c.46-43098T>C VV NP_001350830.1:p.=
NM_001363903.1:c.46-43098T>C VV NP_001350832.1:p.=
NM_001363905.1:c.-647-43098T>C VV NP_001350834.1:p.=
NM_001363988.1:c.46-43098T>C VV NP_001350917.1:p.=
NR_156761.1:n.268-43098T>C
XM_011523314.3:c.46-43098T>C
XM_011523315.3:c.46-43098T>C
XM_011523316.3:c.46-43098T>C
XM_017023654.2:c.46-43098T>C XP_016879143.1:p.=
XM_017023655.2:c.46-43098T>C XP_016879144.1:p.=
XM_017023656.2:c.46-43098T>C XP_016879145.1:p.=
XM_017023657.2:c.46-43098T>C XP_016879146.1:p.=
XM_017023658.2:c.46-43098T>C XP_016879147.1:p.=
XM_024450437.1:c.46-43098T>C XP_024306205.1:p.=
XR_002957840.1:n.89-43098T>C
ENST00000464071.1:c.46-43098T>C ENSP00000418424.1:p.=
ENST00000471389.5:c.46-43098T>C ENSP00000418823.1:p.=
ENST00000570395.1:n.193+2762T>C