Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000024.10:g.2866805T>C , CM000686.2:g.2866805T>C | GRCh38 |
| NC_000024.9:g.2734846T>C , CM000686.1:g.2734846T>C | GRCh37 |
| NC_000024.8:g.2794846T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000250784.13:c.703T>C MANE Select | ENSP00000250784.7:p.Trp235Arg | |
| ENST00000250784.12:c.703T>C | ENSP00000250784.7:p.Trp235Arg | |
| ENST00000430575.1:c.730T>C | ENSP00000415317.1:p.Trp244Arg | |
| ENST00000477725.1:n.847T>C | ||
| ENST00000515575.1:n.42+12034T>C | ||
| NM_001008.3:c.703T>C | NP_000999.1:p.Trp235Arg | |
| NM_001008.4:c.703T>C MANE Select | NP_000999.1:p.Trp235Arg |