Linked Data
dbSNP Id:
rs1656913052
gnomAD v4:
1-119140732-C-T
MyVariant Identifiers:
chr1:g.119683355C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.119140732C>T , CM000663.2:g.119140732C>T | GRCh38 |
| NC_000001.10:g.119683355C>T , CM000663.1:g.119683355C>T | GRCh37 |
| NC_000001.9:g.119484878C>T | NCBI36 |
| NG_050658.1:g.5057G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_125974.1:n.337C>T (WARS2-AS1) | ||
| NR_125975.1:n.337C>T (WARS2-AS1) | ||
| NR_125976.1:n.337C>T (WARS2-AS1) | ||
| NR_125977.1:n.337C>T (WARS2-AS1) | ||
| XM_006710283.1:c.-657G>A (WARS2) | XP_006710346.1:n.-657G>A | |
| XM_011540493.1:c.-529G>A (WARS2) | XP_011538795.1:n.-529G>A | |
| XM_011540495.1:c.-88G>A (WARS2) | XP_011538797.1:n.-88G>A | |
| XM_017000041.2:c.-657G>A (WARS2) | XP_016855530.1:n.-657G>A | |
| XM_024449826.1:c.-529G>A (WARS2) | XP_024305594.1:n.-529G>A | |
| XM_024449860.1:c.-657G>A (WARS2) | XP_024305628.1:n.-657G>A |