Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.45804409A>G , CM000681.2:g.45804409A>G | GRCh38 |
| NC_000019.9:g.46307667A>G , CM000681.1:g.46307667A>G | GRCh37 |
| NC_000019.8:g.50999507A>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000221538.8:c.1496T>C MANE Select | ENSP00000221538.2:p.Phe499Ser | |
| ENST00000221538.7:c.1496T>C | ENSP00000221538.2:p.Phe499Ser | |
| ENST00000597055.1:c.1496T>C | ENSP00000472630.1:p.Phe499Ser | |
| ENST00000600188.5:c.704T>C | ENSP00000471559.1:p.Phe235Ser | |
| NM_030785.3:c.1496T>C | NP_110412.1:p.Phe499Ser | |
| XM_011527351.1:c.1496T>C | XP_011525653.1:p.Phe499Ser | |
| XM_011527351.2:c.1496T>C | XP_011525653.1:p.Phe499Ser | |
| NM_030785.4:c.1496T>C MANE Select | NP_110412.1:p.Phe499Ser |