Canonical Allele Identifier: CA420069333
Gene: WARS2 HGNC NCBI
WARS2-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1450956069

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.119140649A>G , CM000663.2:g.119140649A>G GRCh38
NC_000001.10:g.119683272A>G , CM000663.1:g.119683272A>G GRCh37
NC_000001.9:g.119484795A>G NCBI36
NG_050658.1:g.5140T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000235521.5:c.-5T>C (WARS2) MANE Select ENSP00000235521.4:n.-5T>C
ENST00000235521.4:c.-5T>C (WARS2) ENSP00000235521.4:n.-5T>C
ENST00000495746.5:n.6T>C (WARS2)
NM_015836.3:c.-5T>C (WARS2) NP_056651.1:n.-5T>C
NM_201263.2:c.-5T>C (WARS2) NP_957715.1:n.-5T>C
NR_125974.1:n.254A>G (WARS2-AS1)
NR_125975.1:n.254A>G (WARS2-AS1)
NR_125976.1:n.254A>G (WARS2-AS1)
NR_125977.1:n.254A>G (WARS2-AS1)
XM_006710283.1:c.-574T>C (WARS2) XP_006710346.1:n.-574T>C
XM_011540493.1:c.-446T>C (WARS2) XP_011538795.1:n.-446T>C
XM_011540495.1:c.-5T>C (WARS2) XP_011538797.1:n.-5T>C
XM_011540494.2:c.-159T>C (WARS2) XP_011538796.1:n.-159T>C
XM_011540495.2:c.-5T>C (WARS2) XP_011538797.1:n.-5T>C
XM_017000038.1:c.-5T>C (WARS2) XP_016855527.1:n.-5T>C
XM_017000039.1:c.-350T>C (WARS2) XP_016855528.1:n.-350T>C
XM_017000040.1:c.-5T>C (WARS2) XP_016855529.1:n.-5T>C
XM_017000041.2:c.-574T>C (WARS2) XP_016855530.1:n.-574T>C
XM_017000042.1:c.-5T>C (WARS2) XP_016855531.1:n.-5T>C
XM_024449826.1:c.-446T>C (WARS2) XP_024305594.1:n.-446T>C
XM_024449860.1:c.-574T>C (WARS2) XP_024305628.1:n.-574T>C
XM_024449871.1:c.-478T>C (WARS2) XP_024305639.1:n.-478T>C
NM_001378226.1:c.-159T>C (WARS2) NP_001365155.1:n.-159T>C
NM_001378227.1:c.-350T>C (WARS2) NP_001365156.1:n.-350T>C
NM_001378228.1:c.-5T>C (WARS2) NP_001365157.1:n.-5T>C
NM_001378229.1:c.-5T>C (WARS2) NP_001365158.1:n.-5T>C
NM_001378230.1:c.-478T>C (WARS2) NP_001365159.1:n.-478T>C
NM_001378231.1:c.-5T>C (WARS2) NP_001365160.1:n.-5T>C
NM_015836.4:c.-5T>C (WARS2) MANE Select NP_056651.1:n.-5T>C