Linked Data
dbSNP Id:
rs1026968898
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.136046400A>G , CM000667.2:g.136046400A>G | GRCh38 |
| NC_000005.9:g.135382089A>G , CM000667.1:g.135382089A>G | GRCh37 |
| NC_000005.8:g.135409988A>G | NCBI36 |
| NG_012646.1:g.22506A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000442011.7:c.364A>G MANE Select | ENSP00000416330.2:p.Thr122Ala | |
| ENST00000442011.6:c.364A>G | ENSP00000416330.2:p.Thr122Ala | |
| ENST00000504185.5:n.521A>G | ||
| ENST00000506699.5:n.429A>G | ||
| ENST00000507018.5:c.281A>G | ||
| ENST00000515433.1:n.656A>G | ||
| NM_000358.2:c.364A>G | NP_000349.1:p.Thr122Ala | |
| NM_000358.3:c.364A>G MANE Select | NP_000349.1:p.Thr122Ala |