Linked Data
MyVariant Identifiers:
chr1:g.120295904T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.119753281T>G , CM000663.2:g.119753281T>G | GRCh38 |
| NC_000001.10:g.120295904T>G , CM000663.1:g.120295904T>G | GRCh37 |
| NC_000001.9:g.120097427T>G | NCBI36 |
| NG_013348.1:g.20652A>C , LRG_447:g.20652A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000369406.8:c.1293A>C MANE Select | ENSP00000358414.3:p.Pro431= | |
| ENST00000369406.7:c.1293A>C | ENSP00000358414.3:p.Pro431= | |
| ENST00000544913.2:c.1167A>C | ENSP00000439495.2:p.Pro389= | |
| NM_001166107.1:c.1167A>C , LRG_447t2:c.1167A>C | NP_001159579.1:p.Pro389= | |
| NM_005518.3:c.1293A>C , LRG_447t1:c.1293A>C | NP_005509.1:p.Pro431= | |
| XM_011541313.1:c.1128A>C | XP_011539615.1:p.Pro376= | |
| XM_011541313.2:c.1128A>C | XP_011539615.1:p.Pro376= | |
| NM_005518.4:c.1293A>C MANE Select | NP_005509.1:p.Pro431= |