Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.2445478T>C , CM000673.2:g.2445478T>C | GRCh38 |
| NC_000011.9:g.2466708T>C , CM000673.1:g.2466708T>C | GRCh37 |
| NC_000011.8:g.2423284T>C | NCBI36 |
| NG_008935.1:g.5488T>C , LRG_287:g.5488T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000496887.7:c.119T>C | ENSP00000434560.2:p.Phe40Ser | |
| ENST00000646564.2:c.380T>C | ENSP00000495806.2:p.Phe127Ser | |
| ENST00000155840.12:c.380T>C MANE Select | ENSP00000155840.2:p.Phe127Ser | |
| ENST00000646564.1:c.26T>C | ENSP00000495806.1:p.Phe9Ser | |
| ENST00000155840.9:c.380T>C | ENSP00000155840.2:p.Phe127Ser | |
| ENST00000345015.4:n.157T>C | ||
| ENST00000496887.6:c.119T>C | ENSP00000434560.1:p.Phe40Ser | |
| NM_000218.2:c.380T>C , LRG_287t1:c.380T>C | NP_000209.2:p.Phe127Ser | |
| NM_000218.3:c.380T>C MANE Select | NP_000209.2:p.Phe127Ser |