Linked Data
ClinVar Variation Id:
1761147
ClinVar RCV Id:
RCV002412372
MyVariant Identifiers:
chr6:g.7585397A>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.7585164A>T , CM000668.2:g.7585164A>T | GRCh38 |
| NC_000006.11:g.7585397A>T , CM000668.1:g.7585397A>T | GRCh37 |
| NC_000006.10:g.7530396A>T | NCBI36 |
| NG_008803.1:g.48528A>T , LRG_423:g.48528A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000710359.1:c.6573A>T | ENSP00000518230.1:p.Thr2191= | |
| ENST00000379802.8:c.7902A>T MANE Select | ENSP00000369129.3:p.Thr2634= | |
| ENST00000379802.7:c.7902A>T | ENSP00000369129.3:p.Thr2634= | |
| ENST00000418664.2:c.6105A>T | ENSP00000396591.2:p.Thr2035= | |
| NM_001008844.1:c.6105A>T | NP_001008844.1:p.Thr2035= | |
| NM_004415.2:c.7902A>T , LRG_423t1:c.7902A>T | NP_004406.2:p.Thr2634= | |
| XM_011514323.1:c.6573A>T | XP_011512625.1:p.Thr2191= | |
| NM_001008844.2:c.6105A>T | NP_001008844.1:p.Thr2035= | |
| NM_001319034.1:c.6573A>T | NP_001305963.1:p.Thr2191= | |
| NM_004415.3:c.7902A>T | NP_004406.2:p.Thr2634= | |
| NM_004415.4:c.7902A>T MANE Select | NP_004406.2:p.Thr2634= | |
| NM_001008844.3:c.6105A>T | NP_001008844.1:p.Thr2035= | |
| NM_001319034.2:c.6573A>T | NP_001305963.1:p.Thr2191= |