Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.763863T>C , CM000673.2:g.763863T>C | GRCh38 |
| NC_000011.9:g.763863T>C , CM000673.1:g.763863T>C | GRCh37 |
| NC_000011.8:g.753863T>C | NCBI36 |
| NG_008160.1:g.21432T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000319006.8:c.754T>C MANE Select | ENSP00000321259.3:p.Phe252Leu | |
| ENST00000319006.7:c.754T>C | ENSP00000321259.3:p.Phe252Leu | |
| ENST00000528097.5:c.754T>C | ENSP00000437098.1:p.Phe252Leu | |
| NM_006755.1:c.754T>C | NP_006746.1:p.Phe252Leu | |
| NM_006755.2:c.754T>C MANE Select | NP_006746.1:p.Phe252Leu |