Linked Data
MyVariant Identifiers:
chr10:g.124266249C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.122506733C>A , CM000672.2:g.122506733C>A | GRCh38 |
| NC_000010.10:g.124266249C>A , CM000672.1:g.124266249C>A | GRCh37 |
| NC_000010.9:g.124256239C>A | NCBI36 |
| NG_011554.1:g.50209C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000368984.8:c.820C>A MANE Select | ENSP00000357980.3:p.Arg274= | |
| ENST00000648167.1:c.502C>A | ENSP00000498033.1:p.Arg168= | |
| ENST00000368984.7:c.820C>A | ENSP00000357980.3:p.Arg274= | |
| ENST00000420892.1:c.43C>A | ENSP00000412676.1:p.Arg15= | |
| NM_002775.4:c.820C>A | NP_002766.1:p.Arg274= | |
| NM_002775.5:c.820C>A MANE Select | NP_002766.1:p.Arg274= |