Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.98541877G>T , CM000671.2:g.98541877G>T | GRCh38 |
| NC_000009.11:g.101304159G>T , CM000671.1:g.101304159G>T | GRCh37 |
| NC_000009.10:g.100343980G>T | NCBI36 |
| NG_016426.1:g.172321C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000259455.4:c.626C>A MANE Select | ENSP00000259455.2:p.Ser209Tyr | |
| ENST00000637410.1:n.404C>A | ||
| ENST00000259455.3:c.626C>A | ENSP00000259455.2:p.Ser209Tyr | |
| ENST00000477471.1:n.413C>A | ||
| ENST00000634227.1:n.400C>A | ||
| NM_005458.7:c.626C>A | NP_005449.5:p.Ser209Tyr | |
| XM_017015331.2:c.332C>A | XP_016870820.1:p.Ser111Tyr | |
| NM_005458.8:c.626C>A MANE Select | NP_005449.5:p.Ser209Tyr |