Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.49016075A>T , CM000681.2:g.49016075A>T | GRCh38 |
| NC_000019.9:g.49519332A>T , CM000681.1:g.49519332A>T | GRCh37 |
| NC_000019.8:g.54211144A>T | NCBI36 |
| NG_011464.1:g.6016T>A | |
| NG_033041.1:g.27177A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000649238.3:c.419T>A MANE Select | ENSP00000497294.2:p.Phe140Tyr | |
| ENST00000649284.1:n.510T>A | ||
| ENST00000221421.6:c.419T>A | ENSP00000221421.1:p.Phe140Tyr | |
| ENST00000391869.4:c.409T>A | ENSP00000375742.4:p.Ser137Thr | |
| NM_000894.2:c.419T>A | NP_000885.1:p.Phe140Tyr | |
| XM_011526975.1:c.467T>A | XP_011525277.1:p.Phe156Tyr | |
| NM_000894.3:c.419T>A MANE Select | NP_000885.1:p.Phe140Tyr |