Canonical Allele Identifier: CA420069621

Gene: WARS2-AS1 WARS2

Linked Data

• dbSNP Id: rs1360278991
• gnomAD v2: 1-119683315-A-G
• gnomAD v4: 1-119140692-A-G
• MyVariant Identifiers: chr1:g.119683315A>G (hg19) ; chr1:g.119140692A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.119140692A>G , CM000663.2:g.119140692A>G	GRCh38
NC_000001.10:g.119683315A>G , CM000663.1:g.119683315A>G	GRCh37
NC_000001.9:g.119484838A>G	NCBI36
NG_050658.1:g.5097T>C

Transcript Alleles

HGVS	Amino-acid Change
NR_125974.1:n.297A>G (WARS2-AS1)
NR_125975.1:n.297A>G (WARS2-AS1)
NR_125976.1:n.297A>G (WARS2-AS1)
NR_125977.1:n.297A>G (WARS2-AS1)
XM_006710283.1:c.-617T>C (WARS2)	XP_006710346.1:n.-617T>C
XM_011540493.1:c.-489T>C (WARS2)	XP_011538795.1:n.-489T>C
XM_011540495.1:c.-48T>C (WARS2)	XP_011538797.1:n.-48T>C
XM_011540495.2:c.-48T>C (WARS2)	XP_011538797.1:n.-48T>C
XM_017000041.2:c.-617T>C (WARS2)	XP_016855530.1:n.-617T>C
XM_024449826.1:c.-489T>C (WARS2)	XP_024305594.1:n.-489T>C
XM_024449860.1:c.-617T>C (WARS2)	XP_024305628.1:n.-617T>C