Canonical Allele Identifier: CA30387465

Gene: WARS2-AS1 WARS2

Linked Data

• dbSNP Id: rs1019606266
• gnomAD v2: 1-119683301-A-G
• gnomAD v3: 1-119140678-A-G
• gnomAD v4: 1-119140678-A-G
• MyVariant Identifiers: chr1:g.119683301A>G (hg19) ; chr1:g.119140678A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.119140678A>G , CM000663.2:g.119140678A>G	GRCh38
NC_000001.10:g.119683301A>G , CM000663.1:g.119683301A>G	GRCh37
NC_000001.9:g.119484824A>G	NCBI36
NG_050658.1:g.5111T>C

Transcript Alleles

HGVS	Amino-acid Change
NR_125974.1:n.283A>G (WARS2-AS1)
NR_125975.1:n.283A>G (WARS2-AS1)
NR_125976.1:n.283A>G (WARS2-AS1)
NR_125977.1:n.283A>G (WARS2-AS1)
XM_006710283.1:c.-603T>C (WARS2)	XP_006710346.1:n.-603T>C
XM_011540493.1:c.-475T>C (WARS2)	XP_011538795.1:n.-475T>C
XM_011540495.1:c.-34T>C (WARS2)	XP_011538797.1:n.-34T>C
XM_011540495.2:c.-34T>C (WARS2)	XP_011538797.1:n.-34T>C
XM_017000041.2:c.-603T>C (WARS2)	XP_016855530.1:n.-603T>C
XM_024449826.1:c.-475T>C (WARS2)	XP_024305594.1:n.-475T>C
XM_024449860.1:c.-603T>C (WARS2)	XP_024305628.1:n.-603T>C