Linked Data
MyVariant Identifiers:
chr15:g.75047192T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.74754851T>C , CM000677.2:g.74754851T>C | GRCh38 |
| NC_000015.9:g.75047192T>C , CM000677.1:g.75047192T>C | GRCh37 |
| NC_000015.8:g.72834245T>C | NCBI36 |
| NG_008431.1:g.37310T>C | |
| NG_008431.2:g.37310T>C | |
| NG_061543.1:g.11007T>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000343932.5:c.1314T>C MANE Select | ENSP00000342007.4:p.Thr438= | |
| ENST00000343932.4:c.1314T>C | ENSP00000342007.4:p.Thr438= | |
| NM_000761.4:c.1314T>C | NP_000752.2:p.Thr438= | |
| NM_000761.5:c.1314T>C MANE Select | NP_000752.2:p.Thr438= |