Canonical Allele Identifier: CA1035438

Gene: WARS2 WARS2-AS1

Linked Data

• dbSNP Id: rs775078734
• ExAC: 1:119683289 T / A
• gnomAD v2: 1-119683289-T-A
• gnomAD v4: 1-119140666-T-A
• MyVariant Identifiers: chr1:g.119683289T>A (hg19) ; chr1:g.119140666T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.119140666T>A , CM000663.2:g.119140666T>A	GRCh38
NC_000001.10:g.119683289T>A , CM000663.1:g.119683289T>A	GRCh37
NC_000001.9:g.119484812T>A	NCBI36
NG_050658.1:g.5123A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000235521.4:c.-22A>T (WARS2)	ENSP00000235521.4:n.-22A>T
NM_015836.3:c.-22A>T (WARS2)	NP_056651.1:n.-22A>T
NM_201263.2:c.-22A>T (WARS2)	NP_957715.1:n.-22A>T
NR_125974.1:n.271T>A (WARS2-AS1)
NR_125975.1:n.271T>A (WARS2-AS1)
NR_125976.1:n.271T>A (WARS2-AS1)
NR_125977.1:n.271T>A (WARS2-AS1)
XM_006710283.1:c.-591A>T (WARS2)	XP_006710346.1:n.-591A>T
XM_011540493.1:c.-463A>T (WARS2)	XP_011538795.1:n.-463A>T
XM_011540495.1:c.-22A>T (WARS2)	XP_011538797.1:n.-22A>T
XM_011540495.2:c.-22A>T (WARS2)	XP_011538797.1:n.-22A>T
XM_017000041.2:c.-591A>T (WARS2)	XP_016855530.1:n.-591A>T
XM_024449826.1:c.-463A>T (WARS2)	XP_024305594.1:n.-463A>T
XM_024449860.1:c.-591A>T (WARS2)	XP_024305628.1:n.-591A>T