Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.165069155T>A , CM000665.2:g.165069155T>A | GRCh38 |
| NC_000003.11:g.164786943T>A , CM000665.1:g.164786943T>A | GRCh37 |
| NC_000003.10:g.166269637T>A | NCBI36 |
| NG_017043.1:g.14341A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264382.8:c.296A>T MANE Select | ENSP00000264382.3:p.Asn99Ile | |
| ENST00000264382.7:c.296A>T | ENSP00000264382.3:p.Asn99Ile | |
| ENST00000476593.1:c.*171A>T | ENSP00000419450.1:n.*171A>T | |
| NM_001041.3:c.296A>T | NP_001032.2:p.Asn99Ile | |
| XM_011513078.1:c.197A>T | XP_011511380.1:p.Asn66Ile | |
| XM_011513078.2:c.197A>T | XP_011511380.1:p.Asn66Ile | |
| NM_001041.4:c.296A>T MANE Select | NP_001032.2:p.Asn99Ile |