Linked Data
dbSNP Id:
rs969056253
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.100734316A>T , CM000676.2:g.100734316A>T | GRCh38 |
| NC_000014.8:g.101200653A>T , CM000676.1:g.101200653A>T | GRCh37 |
| NC_000014.7:g.100270406A>T | NCBI36 |
| NG_016863.2:g.12452A>T | |
| NG_016863.3:g.12452A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000341267.9:c.572A>T MANE Select | ENSP00000340292.4:p.Asp191Val | |
| ENST00000331224.10:c.572A>T | ENSP00000331081.6:p.Asp191Val | |
| ENST00000341267.8:c.572A>T | ENSP00000340292.4:p.Asp191Val | |
| NM_003836.5:c.572A>T | NP_003827.3:p.Asp191Val | |
| NM_001317172.1:c.572A>T | NP_001304101.1:p.Asp191Val | |
| NM_003836.6:c.572A>T | NP_003827.3:p.Asp191Val | |
| NM_001317172.2:c.572A>T | NP_001304101.2:p.Asp191Val | |
| NM_003836.7:c.572A>T MANE Select | NP_003827.4:p.Asp191Val |