Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.31860560T>A , CM000668.2:g.31860560T>A | GRCh38 |
| NC_000006.11:g.31828337T>A , CM000668.1:g.31828337T>A | GRCh37 |
| NC_000006.10:g.31936316T>A | NCBI36 |
| NG_008201.1:g.7373A>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000375631.5:c.677A>T MANE Select | ENSP00000364782.4:p.Asp226Val | |
| ENST00000677054.1:n.1920A>T | ||
| ENST00000677512.1:n.785A>T | ||
| ENST00000678869.1:n.1351A>T | ||
| ENST00000375631.4:c.677A>T | ENSP00000364782.4:p.Asp226Val | |
| ENST00000480384.1:n.706A>T | ||
| ENST00000491768.5:c.677A>T | ENSP00000433127.1:p.Asp226Val | |
| ENST00000495807.1:n.1811A>T | ||
| NM_000434.3:c.677A>T | NP_000425.1:p.Asp226Val | |
| NM_000434.4:c.677A>T MANE Select | NP_000425.1:p.Asp226Val |