Linked Data
MyVariant Identifiers:
chr1:g.169511067G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.169541829G>A , CM000663.2:g.169541829G>A | GRCh38 |
| NC_000001.10:g.169511067G>A , CM000663.1:g.169511067G>A | GRCh37 |
| NC_000001.9:g.167777691G>A | NCBI36 |
| NG_011806.1:g.49703C>T , LRG_553:g.49703C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000367797.9:c.3261C>T MANE Select | ENSP00000356771.3:p.Pro1087= | |
| ENST00000367796.3:c.3276C>T | ENSP00000356770.3:p.Pro1092= | |
| ENST00000367797.7:c.3261C>T | ENSP00000356771.3:p.Pro1087= | |
| NM_000130.4:c.3261C>T , LRG_553t1:c.3261C>T | NP_000121.2:p.Pro1087= | |
| XM_017000660.2:c.2850C>T | XP_016856149.1:p.Pro950= | |
| NM_000130.5:c.3261C>T MANE Select | NP_000121.2:p.Pro1087= |