Linked Data
MyVariant Identifiers:
chr10:g.124266230T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.122506714T>C , CM000672.2:g.122506714T>C | GRCh38 |
| NC_000010.10:g.124266230T>C , CM000672.1:g.124266230T>C | GRCh37 |
| NC_000010.9:g.124256220T>C | NCBI36 |
| NG_011554.1:g.50190T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000368984.8:c.801T>C MANE Select | ENSP00000357980.3:p.Leu267= | |
| ENST00000648167.1:c.483T>C | ENSP00000498033.1:p.Leu161= | |
| ENST00000368984.7:c.801T>C | ENSP00000357980.3:p.Leu267= | |
| ENST00000420892.1:c.24T>C | ENSP00000412676.1:p.Leu8= | |
| NM_002775.4:c.801T>C | NP_002766.1:p.Leu267= | |
| NM_002775.5:c.801T>C MANE Select | NP_002766.1:p.Leu267= |