Linked Data
MyVariant Identifiers:
chr1:g.169521879G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.169552641G>A , CM000663.2:g.169552641G>A | GRCh38 |
| NC_000001.10:g.169521879G>A , CM000663.1:g.169521879G>A | GRCh37 |
| NC_000001.9:g.167788503G>A | NCBI36 |
| NG_011806.1:g.38891C>T , LRG_553:g.38891C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000367797.9:c.1212C>T MANE Select | ENSP00000356771.3:p.Phe404= | |
| ENST00000367796.3:c.1212C>T | ENSP00000356770.3:p.Phe404= | |
| ENST00000367797.7:c.1212C>T | ENSP00000356771.3:p.Phe404= | |
| NM_000130.4:c.1212C>T , LRG_553t1:c.1212C>T | NP_000121.2:p.Phe404= | |
| XM_017000660.2:c.801C>T | XP_016856149.1:p.Phe267= | |
| NM_000130.5:c.1212C>T MANE Select | NP_000121.2:p.Phe404= |