Linked Data
MyVariant Identifiers:
chr4:g.120241879A>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.119320724A>C , CM000666.2:g.119320724A>C | GRCh38 |
| NC_000004.11:g.120241879A>C , CM000666.1:g.120241879A>C | GRCh37 |
| NC_000004.10:g.120461327A>C | NCBI36 |
| NG_011444.1:g.6438T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000274024.4:c.186T>G MANE Select | ENSP00000274024.3:p.Val62= | |
| ENST00000274024.3:c.186T>G | ENSP00000274024.3:p.Val62= | |
| NM_000134.3:c.186T>G | NP_000125.2:p.Val62= | |
| NM_000134.4:c.186T>G MANE Select | NP_000125.2:p.Val62= |