Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.142954279A>G , CM000669.2:g.142954279A>G | GRCh38 |
| NC_000007.13:g.142651366A>G , CM000669.1:g.142651366A>G | GRCh37 |
| NC_000007.12:g.142361488A>G | NCBI36 |
| NG_007492.1:g.13138T>C | |
| NG_007492.2:g.13138T>C | |
| NG_007492.3:g.13138T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000355265.7:c.829T>C MANE Select | ENSP00000347409.2:p.Ser277Pro | |
| ENST00000355265.6:c.829T>C | ENSP00000347409.2:p.Ser277Pro | |
| ENST00000479768.6:n.947T>C | ||
| NM_000420.2:c.829T>C | NP_000411.1:p.Ser277Pro | |
| XM_005249993.2:c.865T>C | XP_005250050.1:p.Ser289Pro | |
| XM_005249994.3:c.-119T>C | XP_005250051.1:n.-119T>C | |
| NM_000420.3:c.829T>C MANE Select | NP_000411.1:p.Ser277Pro |