Canonical Allele Identifier: CA10780120
Gene: WARS2-AS1 HGNC NCBI
WARS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1178536
ClinVar RCV Id: RCV001534841
dbSNP Id: rs12096448
gnomAD v2: 1-119683390-G-A
gnomAD v3: 1-119140767-G-A
gnomAD v4: 1-119140767-G-A
MyVariant Identifiers: chr1:g.119683390G>A (hg19) chr1:g.119140767G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.119140767G>A , CM000663.2:g.119140767G>A GRCh38
NC_000001.10:g.119683390G>A , CM000663.1:g.119683390G>A GRCh37
NC_000001.9:g.119484913G>A NCBI36
NG_050658.1:g.5022C>T

Transcript Alleles

HGVS Amino-acid Change
NR_125974.1:n.372G>A (WARS2-AS1)
NR_125975.1:n.372G>A (WARS2-AS1)
NR_125976.1:n.372G>A (WARS2-AS1)
NR_125977.1:n.372G>A (WARS2-AS1)
XM_006710283.1:c.-692C>T (WARS2) XP_006710346.1:n.-692C>T
XM_011540493.1:c.-564C>T (WARS2) XP_011538795.1:n.-564C>T
XM_011540495.1:c.-123C>T (WARS2) XP_011538797.1:n.-123C>T
XM_017000041.2:c.-692C>T (WARS2) XP_016855530.1:n.-692C>T
XM_024449826.1:c.-564C>T (WARS2) XP_024305594.1:n.-564C>T
XM_024449860.1:c.-692C>T (WARS2) XP_024305628.1:n.-692C>T
Search 100 bp 5'
Search 100 bp 3'