Canonical Allele Identifier: CA362735945
Gene: FARS2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.5404664A>C , CM000668.2:g.5404664A>C GRCh38
NC_000006.11:g.5404897A>C , CM000668.1:g.5404897A>C GRCh37
NC_000006.10:g.5349896A>C NCBI36
NG_033003.1:g.148314A>C
NG_033003.2:g.148314A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000274680.9:c.735A>C MANE Select ENSP00000274680.4:p.Gln245His
ENST00000648580.1:c.735A>C ENSP00000497889.1:p.Gln245His
ENST00000274680.8:c.735A>C ENSP00000274680.3:p.Gln245His
ENST00000324331.10:c.735A>C ENSP00000316335.5:p.Gln245His
ENST00000445533.1:c.123A>C ENSP00000392525.1:p.Gln41His
NM_006567.3:c.735A>C NP_006558.1:p.Gln245His
XM_005248811.1:c.735A>C XP_005248868.1:p.Gln245His
XM_005248812.2:c.735A>C XP_005248869.1:p.Gln245His
XM_006714966.1:c.735A>C XP_006715029.1:p.Gln245His
XM_011514247.1:c.735A>C XP_011512549.1:p.Gln245His
XM_011514248.1:c.735A>C XP_011512550.1:p.Gln245His
XM_011514249.1:c.735A>C XP_011512551.1:p.Gln245His
XM_011514250.1:c.735A>C XP_011512552.1:p.Gln245His
XM_011514251.1:c.735A>C XP_011512553.1:p.Gln245His
XR_926026.1:n.1066A>C
XR_926027.1:n.1066A>C
XR_926028.1:n.1066A>C
NM_001318872.1:c.735A>C NP_001305801.1:p.Gln245His
NM_006567.4:c.735A>C NP_006558.1:p.Gln245His
XM_005248812.3:c.735A>C XP_005248869.1:p.Gln245His
XM_006714966.3:c.735A>C XP_006715029.1:p.Gln245His
XM_011514247.3:c.735A>C XP_011512549.1:p.Gln245His
XM_011514248.3:c.735A>C XP_011512550.1:p.Gln245His
XM_011514249.2:c.735A>C XP_011512551.1:p.Gln245His
XM_011514251.3:c.735A>C XP_011512553.1:p.Gln245His
XM_017010186.1:c.735A>C XP_016865675.1:p.Gln245His
XM_017010187.1:c.735A>C XP_016865676.1:p.Gln245His
XR_926027.3:n.1043A>C
XR_926028.2:n.1043A>C
NM_001318872.2:c.735A>C NP_001305801.1:p.Gln245His
NM_001374875.1:c.735A>C NP_001361804.1:p.Gln245His
NM_001374876.1:c.735A>C NP_001361805.1:p.Gln245His
NM_001374877.1:c.735A>C NP_001361806.1:p.Gln245His
NM_001374878.1:c.735A>C NP_001361807.1:p.Gln245His
NM_001374879.1:c.735A>C NP_001361808.1:p.Gln245His
NM_001375257.1:c.735A>C NP_001362186.1:p.Gln245His
NM_001375258.1:c.735A>C NP_001362187.1:p.Gln245His
NM_001375259.1:c.39A>C NP_001362188.1:p.Gln13His
NM_001375260.1:c.39A>C NP_001362189.1:p.Gln13His
NM_006567.5:c.735A>C MANE Select NP_006558.1:p.Gln245His