Canonical Allele Identifier: CA420069335

Gene: WARS2 WARS2-AS1

Linked Data

• dbSNP Id: rs1656905895
• MyVariant Identifiers: chr1:g.119683273G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.119140650G>A , CM000663.2:g.119140650G>A	GRCh38
NC_000001.10:g.119683273G>A , CM000663.1:g.119683273G>A	GRCh37
NC_000001.9:g.119484796G>A	NCBI36
NG_050658.1:g.5139C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000235521.5:c.-6C>T (WARS2) MANE Select	ENSP00000235521.4:n.-6C>T
ENST00000235521.4:c.-6C>T (WARS2)	ENSP00000235521.4:n.-6C>T
ENST00000495746.5:n.5C>T (WARS2)
NM_015836.3:c.-6C>T (WARS2)	NP_056651.1:n.-6C>T
NM_201263.2:c.-6C>T (WARS2)	NP_957715.1:n.-6C>T
NR_125974.1:n.255G>A (WARS2-AS1)
NR_125975.1:n.255G>A (WARS2-AS1)
NR_125976.1:n.255G>A (WARS2-AS1)
NR_125977.1:n.255G>A (WARS2-AS1)
XM_006710283.1:c.-575C>T (WARS2)	XP_006710346.1:n.-575C>T
XM_011540493.1:c.-447C>T (WARS2)	XP_011538795.1:n.-447C>T
XM_011540495.1:c.-6C>T (WARS2)	XP_011538797.1:n.-6C>T
XM_011540494.2:c.-160C>T (WARS2)	XP_011538796.1:n.-160C>T
XM_011540495.2:c.-6C>T (WARS2)	XP_011538797.1:n.-6C>T
XM_017000038.1:c.-6C>T (WARS2)	XP_016855527.1:n.-6C>T
XM_017000039.1:c.-351C>T (WARS2)	XP_016855528.1:n.-351C>T
XM_017000040.1:c.-6C>T (WARS2)	XP_016855529.1:n.-6C>T
XM_017000041.2:c.-575C>T (WARS2)	XP_016855530.1:n.-575C>T
XM_017000042.1:c.-6C>T (WARS2)	XP_016855531.1:n.-6C>T
XM_024449826.1:c.-447C>T (WARS2)	XP_024305594.1:n.-447C>T
XM_024449860.1:c.-575C>T (WARS2)	XP_024305628.1:n.-575C>T
XM_024449871.1:c.-479C>T (WARS2)	XP_024305639.1:n.-479C>T
NM_001378226.1:c.-160C>T (WARS2)	NP_001365155.1:n.-160C>T
NM_001378227.1:c.-351C>T (WARS2)	NP_001365156.1:n.-351C>T
NM_001378228.1:c.-6C>T (WARS2)	NP_001365157.1:n.-6C>T
NM_001378229.1:c.-6C>T (WARS2)	NP_001365158.1:n.-6C>T
NM_001378230.1:c.-479C>T (WARS2)	NP_001365159.1:n.-479C>T
NM_001378231.1:c.-6C>T (WARS2)	NP_001365160.1:n.-6C>T
NM_015836.4:c.-6C>T (WARS2) MANE Select	NP_056651.1:n.-6C>T