Linked Data
MyVariant Identifiers:
chr5:g.139494363T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.140114778T>G , CM000667.2:g.140114778T>G | GRCh38 |
| NC_000005.9:g.139494363T>G , CM000667.1:g.139494363T>G | GRCh37 |
| NC_000005.8:g.139474547T>G | NCBI36 |
| NG_041813.1:g.5656T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000331327.5:c.597T>G MANE Select | ENSP00000332706.3:p.Arg199= | |
| ENST00000651386.1:c.597T>G | ENSP00000499133.1:p.Arg199= | |
| ENST00000331327.4:c.597T>G | ENSP00000332706.3:p.Arg199= | |
| NM_005859.4:c.597T>G | NP_005850.1:p.Arg199= | |
| NM_005859.5:c.597T>G MANE Select | NP_005850.1:p.Arg199= |