Canonical Allele Identifier: CA341436663

Gene: WARS2

Linked Data

• MyVariant Identifiers: chr1:g.119575850G>C (hg19) ; chr1:g.119033227G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.119033227G>C , CM000663.2:g.119033227G>C	GRCh38
NC_000001.10:g.119575850G>C , CM000663.1:g.119575850G>C	GRCh37
NC_000001.9:g.119377373G>C	NCBI36
NG_050658.1:g.112562C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000235521.5:c.767C>G MANE Select	ENSP00000235521.4:p.Thr256Arg
ENST00000235521.4:c.767C>G	ENSP00000235521.4:p.Thr256Arg
ENST00000369426.9:c.*133C>G	ENSP00000358434.5:n.*133C>G
NM_015836.3:c.767C>G	NP_056651.1:p.Thr256Arg
NM_201263.2:c.*133C>G	NP_957715.1:n.*133C>G
XM_005270350.2:c.713C>G	XP_005270407.1:p.Thr238Arg
XM_006710283.1:c.485C>G	XP_006710346.1:p.Thr162Arg
XM_011540493.1:c.698C>G	XP_011538795.1:p.Thr233Arg
XM_011540494.1:c.698C>G	XP_011538796.1:p.Thr233Arg
XM_011540495.1:c.509C>G	XP_011538797.1:p.Thr170Arg
XM_005270350.3:c.713C>G	XP_005270407.1:p.Thr238Arg
XM_011540494.2:c.698C>G	XP_011538796.1:p.Thr233Arg
XM_011540495.2:c.509C>G	XP_011538797.1:p.Thr170Arg
XM_017000038.1:c.710C>G	XP_016855527.1:p.Thr237Arg
XM_017000039.1:c.698C>G	XP_016855528.1:p.Thr233Arg
XM_017000040.1:c.596C>G	XP_016855529.1:p.Thr199Arg
XM_017000041.2:c.428C>G	XP_016855530.1:p.Thr143Arg
XM_017000042.1:c.*102C>G	XP_016855531.1:n.*102C>G
XM_024449826.1:c.698C>G	XP_024305594.1:p.Thr233Arg
XM_024449860.1:c.485C>G	XP_024305628.1:p.Thr162Arg
XM_024449871.1:c.485C>G	XP_024305639.1:p.Thr162Arg
NM_001378226.1:c.698C>G	NP_001365155.1:p.Thr233Arg
NM_001378227.1:c.698C>G	NP_001365156.1:p.Thr233Arg
NM_001378228.1:c.596C>G	NP_001365157.1:p.Thr199Arg
NM_001378229.1:c.509C>G	NP_001365158.1:p.Thr170Arg
NM_001378230.1:c.485C>G	NP_001365159.1:p.Thr162Arg
NM_001378231.1:c.*102C>G	NP_001365160.1:n.*102C>G
NM_015836.4:c.767C>G MANE Select	NP_056651.1:p.Thr256Arg