Linked Data
MyVariant Identifiers:
chr1:g.169524422G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.169555184G>A , CM000663.2:g.169555184G>A | GRCh38 |
| NC_000001.10:g.169524422G>A , CM000663.1:g.169524422G>A | GRCh37 |
| NC_000001.9:g.167791046G>A | NCBI36 |
| NG_011806.1:g.36348C>T , LRG_553:g.36348C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000367797.9:c.1116C>T MANE Select | ENSP00000356771.3:p.Asp372= | |
| ENST00000367796.3:c.1116C>T | ENSP00000356770.3:p.Asp372= | |
| ENST00000367797.7:c.1116C>T | ENSP00000356771.3:p.Asp372= | |
| NM_000130.4:c.1116C>T , LRG_553t1:c.1116C>T | NP_000121.2:p.Asp372= | |
| XM_017000660.2:c.705C>T | XP_016856149.1:p.Asp235= | |
| NM_000130.5:c.1116C>T MANE Select | NP_000121.2:p.Asp372= |