Canonical Allele Identifier: CA420192632
Gene: WARS2 HGNC NCBI

Linked Data

dbSNP Id: rs1647586485
MyVariant Identifiers: chr1:g.119575810G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.119033187G>A , CM000663.2:g.119033187G>A GRCh38
NC_000001.10:g.119575810G>A , CM000663.1:g.119575810G>A GRCh37
NC_000001.9:g.119377333G>A NCBI36
NG_050658.1:g.112602C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000235521.5:c.807C>T MANE Select ENSP00000235521.4:p.Arg269=
ENST00000235521.4:c.807C>T ENSP00000235521.4:p.Arg269=
ENST00000369426.9:c.*173C>T ENSP00000358434.5:n.*173C>T
NM_015836.3:c.807C>T NP_056651.1:p.Arg269=
NM_201263.2:c.*173C>T NP_957715.1:n.*173C>T
XM_005270350.2:c.753C>T XP_005270407.1:p.Arg251=
XM_006710283.1:c.525C>T XP_006710346.1:p.Arg175=
XM_011540493.1:c.738C>T XP_011538795.1:p.Arg246=
XM_011540494.1:c.738C>T XP_011538796.1:p.Arg246=
XM_011540495.1:c.549C>T XP_011538797.1:p.Arg183=
XM_005270350.3:c.753C>T XP_005270407.1:p.Arg251=
XM_011540494.2:c.738C>T XP_011538796.1:p.Arg246=
XM_011540495.2:c.549C>T XP_011538797.1:p.Arg183=
XM_017000038.1:c.750C>T XP_016855527.1:p.Arg250=
XM_017000039.1:c.738C>T XP_016855528.1:p.Arg246=
XM_017000040.1:c.636C>T XP_016855529.1:p.Arg212=
XM_017000041.2:c.468C>T XP_016855530.1:p.Arg156=
XM_017000042.1:c.*142C>T XP_016855531.1:n.*142C>T
XM_024449826.1:c.738C>T XP_024305594.1:p.Arg246=
XM_024449860.1:c.525C>T XP_024305628.1:p.Arg175=
XM_024449871.1:c.525C>T XP_024305639.1:p.Arg175=
NM_001378226.1:c.738C>T NP_001365155.1:p.Arg246=
NM_001378227.1:c.738C>T NP_001365156.1:p.Arg246=
NM_001378228.1:c.636C>T NP_001365157.1:p.Arg212=
NM_001378229.1:c.549C>T NP_001365158.1:p.Arg183=
NM_001378230.1:c.525C>T NP_001365159.1:p.Arg175=
NM_001378231.1:c.*142C>T NP_001365160.1:n.*142C>T
NM_015836.4:c.807C>T MANE Select NP_056651.1:p.Arg269=