Canonical Allele Identifier: CA362736909
Gene: FARS2 HGNC NCBI

Linked Data

dbSNP Id: rs1305581076

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.5613241G>T , CM000668.2:g.5613241G>T GRCh38
NC_000006.11:g.5613474G>T , CM000668.1:g.5613474G>T GRCh37
NC_000006.10:g.5558473G>T NCBI36
NG_033003.1:g.356891G>T
NG_033003.2:g.356891G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000274680.9:c.1138G>T MANE Select ENSP00000274680.4:p.Asp380Tyr
ENST00000648580.1:c.1138G>T ENSP00000497889.1:p.Asp380Tyr
ENST00000274680.8:c.1138G>T ENSP00000274680.3:p.Asp380Tyr
ENST00000324331.10:c.1138G>T ENSP00000316335.5:p.Asp380Tyr
NM_006567.3:c.1138G>T NP_006558.1:p.Asp380Tyr
XM_005248811.1:c.1138G>T XP_005248868.1:p.Asp380Tyr
XM_005248812.2:c.1138G>T XP_005248869.1:p.Asp380Tyr
XM_011514247.1:c.1138G>T XP_011512549.1:p.Asp380Tyr
XM_011514248.1:c.1138G>T XP_011512550.1:p.Asp380Tyr
XM_011514249.1:c.1138G>T XP_011512551.1:p.Asp380Tyr
XR_926026.1:n.2112G>T
XR_926028.1:n.1601G>T
NM_001318872.1:c.1138G>T NP_001305801.1:p.Asp380Tyr
NM_006567.4:c.1138G>T NP_006558.1:p.Asp380Tyr
XM_005248812.3:c.1138G>T XP_005248869.1:p.Asp380Tyr
XM_011514247.3:c.1138G>T XP_011512549.1:p.Asp380Tyr
XM_011514248.3:c.1138G>T XP_011512550.1:p.Asp380Tyr
XM_011514249.2:c.1138G>T XP_011512551.1:p.Asp380Tyr
XM_017010186.1:c.1138G>T XP_016865675.1:p.Asp380Tyr
XM_017010187.1:c.1138G>T XP_016865676.1:p.Asp380Tyr
XR_926028.2:n.1578G>T
NM_001318872.2:c.1138G>T NP_001305801.1:p.Asp380Tyr
NM_001374875.1:c.1138G>T NP_001361804.1:p.Asp380Tyr
NM_001374876.1:c.1138G>T NP_001361805.1:p.Asp380Tyr
NM_001374877.1:c.1138G>T NP_001361806.1:p.Asp380Tyr
NM_001374878.1:c.1138G>T NP_001361807.1:p.Asp380Tyr
NM_001374879.1:c.1138G>T NP_001361808.1:p.Asp380Tyr
NM_001375257.1:c.1138G>T NP_001362186.1:p.Asp380Tyr
NM_001375258.1:c.1006G>T NP_001362187.1:p.Asp336Tyr
NM_001375259.1:c.442G>T NP_001362188.1:p.Asp148Tyr
NM_001375260.1:c.442G>T NP_001362189.1:p.Asp148Tyr
NM_006567.5:c.1138G>T MANE Select NP_006558.1:p.Asp380Tyr