Linked Data
MyVariant Identifiers:
chr1:g.119683356T>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.119140733T>A , CM000663.2:g.119140733T>A | GRCh38 |
| NC_000001.10:g.119683356T>A , CM000663.1:g.119683356T>A | GRCh37 |
| NC_000001.9:g.119484879T>A | NCBI36 |
| NG_050658.1:g.5056A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_125974.1:n.338T>A (WARS2-AS1) | ||
| NR_125975.1:n.338T>A (WARS2-AS1) | ||
| NR_125976.1:n.338T>A (WARS2-AS1) | ||
| NR_125977.1:n.338T>A (WARS2-AS1) | ||
| XM_006710283.1:c.-658A>T (WARS2) | XP_006710346.1:n.-658A>T | |
| XM_011540493.1:c.-530A>T (WARS2) | XP_011538795.1:n.-530A>T | |
| XM_011540495.1:c.-89A>T (WARS2) | XP_011538797.1:n.-89A>T | |
| XM_017000041.2:c.-658A>T (WARS2) | XP_016855530.1:n.-658A>T | |
| XM_024449826.1:c.-530A>T (WARS2) | XP_024305594.1:n.-530A>T | |
| XM_024449860.1:c.-658A>T (WARS2) | XP_024305628.1:n.-658A>T |