Linked Data
MyVariant Identifiers:
chr5:g.1213598G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.1213483G>T , CM000667.2:g.1213483G>T | GRCh38 |
| NC_000005.9:g.1213598G>T , CM000667.1:g.1213598G>T | GRCh37 |
| NC_000005.8:g.1266598G>T | NCBI36 |
| NG_008282.1:g.16889G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000304460.11:c.684G>T MANE Select | ENSP00000305302.10:p.Thr228= | |
| ENST00000304460.10:c.684G>T | ENSP00000305302.10:p.Thr228= | |
| ENST00000515652.5:c.592G>T | ENSP00000425701.1:p.Ala198Ser | |
| NM_001003841.2:c.684G>T | NP_001003841.1:p.Thr228= | |
| NM_001003841.3:c.684G>T MANE Select | NP_001003841.1:p.Thr228= |