Canonical Allele Identifier: CA420069487

Gene: WARS2 WARS2-AS1

Linked Data

• MyVariant Identifiers: chr1:g.119683294T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.119140671T>G , CM000663.2:g.119140671T>G	GRCh38
NC_000001.10:g.119683294T>G , CM000663.1:g.119683294T>G	GRCh37
NC_000001.9:g.119484817T>G	NCBI36
NG_050658.1:g.5118A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000235521.4:c.-27A>C (WARS2)	ENSP00000235521.4:n.-27A>C
NM_015836.3:c.-27A>C (WARS2)	NP_056651.1:n.-27A>C
NM_201263.2:c.-27A>C (WARS2)	NP_957715.1:n.-27A>C
NR_125974.1:n.276T>G (WARS2-AS1)
NR_125975.1:n.276T>G (WARS2-AS1)
NR_125976.1:n.276T>G (WARS2-AS1)
NR_125977.1:n.276T>G (WARS2-AS1)
XM_006710283.1:c.-596A>C (WARS2)	XP_006710346.1:n.-596A>C
XM_011540493.1:c.-468A>C (WARS2)	XP_011538795.1:n.-468A>C
XM_011540495.1:c.-27A>C (WARS2)	XP_011538797.1:n.-27A>C
XM_011540495.2:c.-27A>C (WARS2)	XP_011538797.1:n.-27A>C
XM_017000041.2:c.-596A>C (WARS2)	XP_016855530.1:n.-596A>C
XM_024449826.1:c.-468A>C (WARS2)	XP_024305594.1:n.-468A>C
XM_024449860.1:c.-596A>C (WARS2)	XP_024305628.1:n.-596A>C