Linked Data
MyVariant Identifiers:
chr1:g.169521858G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.169552620G>T , CM000663.2:g.169552620G>T | GRCh38 |
| NC_000001.10:g.169521858G>T , CM000663.1:g.169521858G>T | GRCh37 |
| NC_000001.9:g.167788482G>T | NCBI36 |
| NG_011806.1:g.38912C>A , LRG_553:g.38912C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000367797.9:c.1233C>A MANE Select | ENSP00000356771.3:p.Pro411= | |
| ENST00000367796.3:c.1233C>A | ENSP00000356770.3:p.Pro411= | |
| ENST00000367797.7:c.1233C>A | ENSP00000356771.3:p.Pro411= | |
| NM_000130.4:c.1233C>A , LRG_553t1:c.1233C>A | NP_000121.2:p.Pro411= | |
| XM_017000660.2:c.822C>A | XP_016856149.1:p.Pro274= | |
| NM_000130.5:c.1233C>A MANE Select | NP_000121.2:p.Pro411= |