Linked Data
dbSNP Id:
rs1656918963
gnomAD v4:
1-119140775-T-G
MyVariant Identifiers:
chr1:g.119683398T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.119140775T>G , CM000663.2:g.119140775T>G | GRCh38 |
| NC_000001.10:g.119683398T>G , CM000663.1:g.119683398T>G | GRCh37 |
| NC_000001.9:g.119484921T>G | NCBI36 |
| NG_050658.1:g.5014A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_125974.1:n.380T>G (WARS2-AS1) | ||
| NR_125975.1:n.380T>G (WARS2-AS1) | ||
| NR_125976.1:n.380T>G (WARS2-AS1) | ||
| NR_125977.1:n.380T>G (WARS2-AS1) | ||
| XM_006710283.1:c.-700A>C (WARS2) | XP_006710346.1:n.-700A>C | |
| XM_011540493.1:c.-572A>C (WARS2) | XP_011538795.1:n.-572A>C | |
| XM_017000041.2:c.-700A>C (WARS2) | XP_016855530.1:n.-700A>C | |
| XM_024449826.1:c.-572A>C (WARS2) | XP_024305594.1:n.-572A>C | |
| XM_024449860.1:c.-700A>C (WARS2) | XP_024305628.1:n.-700A>C |