Linked Data
MyVariant Identifiers:
chr1:g.169511151A>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.169541913A>G , CM000663.2:g.169541913A>G | GRCh38 |
| NC_000001.10:g.169511151A>G , CM000663.1:g.169511151A>G | GRCh37 |
| NC_000001.9:g.167777775A>G | NCBI36 |
| NG_011806.1:g.49619T>C , LRG_553:g.49619T>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000367797.9:c.3177T>C MANE Select | ENSP00000356771.3:p.Phe1059= | |
| ENST00000367796.3:c.3192T>C | ENSP00000356770.3:p.Phe1064= | |
| ENST00000367797.7:c.3177T>C | ENSP00000356771.3:p.Phe1059= | |
| NM_000130.4:c.3177T>C , LRG_553t1:c.3177T>C | NP_000121.2:p.Phe1059= | |
| XM_017000660.2:c.2766T>C | XP_016856149.1:p.Phe922= | |
| NM_000130.5:c.3177T>C MANE Select | NP_000121.2:p.Phe1059= |