MyVariant.info:
GRCh38
chr1:g.169549811C>A
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.169549811C>A , CM000663.2:g.169549811C>A | GRCh38 |
| NG_011806.1:g.41721G>T , LRG_553:g.41721G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000367797.9:c.1601G>T MANE Select | ENSP00000356771.3:p.Arg534Leu | |
| ENST00000367796.3:c.1601G>T | ENSP00000356770.3:p.Arg534Leu | |
| ENST00000367797.7:c.1601G>T | ENSP00000356771.3:p.Arg534Leu | |
| NM_000130.4:c.1601G>T , LRG_553t1:c.1601G>T | NP_000121.2:p.Arg534Leu | |
| XM_017000660.2:c.1190G>T | XP_016856149.1:p.Arg397Leu | |
| NM_000130.5:c.1601G>T MANE Select | NP_000121.2:p.Arg534Leu |