Linked Data
MyVariant Identifiers:
chr4:g.120241825C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.119320670C>T , CM000666.2:g.119320670C>T | GRCh38 |
| NC_000004.11:g.120241825C>T , CM000666.1:g.120241825C>T | GRCh37 |
| NC_000004.10:g.120461273C>T | NCBI36 |
| NG_011444.1:g.6492G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000274024.4:c.240G>A MANE Select | ENSP00000274024.3:p.Arg80= | |
| ENST00000274024.3:c.240G>A | ENSP00000274024.3:p.Arg80= | |
| NM_000134.3:c.240G>A | NP_000125.2:p.Arg80= | |
| NM_000134.4:c.240G>A MANE Select | NP_000125.2:p.Arg80= |