Linked Data
MyVariant Identifiers:
chr9:g.80409481T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.77794565T>G , CM000671.2:g.77794565T>G | GRCh38 |
| NC_000009.11:g.80409481T>G , CM000671.1:g.80409481T>G | GRCh37 |
| NC_000009.10:g.79599301T>G | NCBI36 |
| NG_027904.2:g.241739A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000286548.9:c.633A>C MANE Select | ENSP00000286548.4:p.Ser211= | |
| ENST00000286548.8:c.633A>C | ENSP00000286548.4:p.Ser211= | |
| NM_002072.4:c.633A>C | NP_002063.2:p.Ser211= | |
| XM_017014628.2:c.459A>C | XP_016870117.1:p.Ser153= | |
| NM_002072.5:c.633A>C MANE Select | NP_002063.2:p.Ser211= |