Canonical Allele Identifier: CA324892
Gene: FARS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 214338
dbSNP Id: rs146356199

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.5369076A>T , CM000668.2:g.5369076A>T GRCh38
NC_000006.11:g.5369309A>T , CM000668.1:g.5369309A>T GRCh37
NC_000006.10:g.5314308A>T NCBI36
NG_033003.1:g.112726A>T
NG_033003.2:g.112726A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000274680.9:c.506A>T MANE Select ENSP00000274680.4:p.Asp169Val
ENST00000648580.1:c.506A>T ENSP00000497889.1:p.Asp169Val
ENST00000274680.8:c.506A>T ENSP00000274680.3:p.Asp169Val
ENST00000324331.10:c.506A>T ENSP00000316335.5:p.Asp169Val
NM_006567.3:c.506A>T NP_006558.1:p.Asp169Val
XM_005248811.1:c.506A>T XP_005248868.1:p.Asp169Val
XM_005248812.2:c.506A>T XP_005248869.1:p.Asp169Val
XM_006714966.1:c.506A>T XP_006715029.1:p.Asp169Val
XM_011514247.1:c.506A>T XP_011512549.1:p.Asp169Val
XM_011514248.1:c.506A>T XP_011512550.1:p.Asp169Val
XM_011514249.1:c.506A>T XP_011512551.1:p.Asp169Val
XM_011514250.1:c.506A>T XP_011512552.1:p.Asp169Val
XM_011514251.1:c.506A>T XP_011512553.1:p.Asp169Val
XR_926026.1:n.837A>T
XR_926027.1:n.837A>T
XR_926028.1:n.837A>T
NM_001318872.1:c.506A>T NP_001305801.1:p.Asp169Val
NM_006567.4:c.506A>T NP_006558.1:p.Asp169Val
XM_005248812.3:c.506A>T XP_005248869.1:p.Asp169Val
XM_006714966.3:c.506A>T XP_006715029.1:p.Asp169Val
XM_011514247.3:c.506A>T XP_011512549.1:p.Asp169Val
XM_011514248.3:c.506A>T XP_011512550.1:p.Asp169Val
XM_011514249.2:c.506A>T XP_011512551.1:p.Asp169Val
XM_011514251.3:c.506A>T XP_011512553.1:p.Asp169Val
XM_017010186.1:c.506A>T XP_016865675.1:p.Asp169Val
XM_017010187.1:c.506A>T XP_016865676.1:p.Asp169Val
XR_926027.3:n.814A>T
XR_926028.2:n.814A>T
NM_001318872.2:c.506A>T NP_001305801.1:p.Asp169Val
NM_001374875.1:c.506A>T NP_001361804.1:p.Asp169Val
NM_001374876.1:c.506A>T NP_001361805.1:p.Asp169Val
NM_001374877.1:c.506A>T NP_001361806.1:p.Asp169Val
NM_001374878.1:c.506A>T NP_001361807.1:p.Asp169Val
NM_001374879.1:c.506A>T NP_001361808.1:p.Asp169Val
NM_001375257.1:c.506A>T NP_001362186.1:p.Asp169Val
NM_001375258.1:c.506A>T NP_001362187.1:p.Asp169Val
NM_001375259.1:c.-84-35466A>T NP_001362188.1:p.=
NM_001375260.1:c.-340-27557A>T NP_001362189.1:p.=
NM_006567.5:c.506A>T MANE Select NP_006558.1:p.Asp169Val