Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.131877086A>T , CM000668.2:g.131877086A>T | GRCh38 |
| NC_000006.11:g.132198226A>T , CM000668.1:g.132198226A>T | GRCh37 |
| NC_000006.10:g.132239919A>T | NCBI36 |
| NG_008206.1:g.74071A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000683687.1:n.690A>T | ||
| ENST00000684536.1:n.316A>T | ||
| ENST00000647893.1:c.1818A>T MANE Select | ENSP00000498074.1:p.Lys606Asn | |
| ENST00000647981.1:n.503A>T | ||
| ENST00000650437.1:c.1309A>T | ||
| ENST00000360971.6:c.1818A>T | ENSP00000354238.2:p.Lys606Asn | |
| ENST00000459624.1:n.862A>T | ||
| ENST00000513998.5:c.*655A>T | ENSP00000422424.1:n.*655A>T | |
| NM_006208.2:c.1818A>T | NP_006199.2:p.Lys606Asn | |
| XM_011535896.1:c.708A>T | XP_011534198.1:p.Lys236Asn | |
| NM_006208.3:c.1818A>T MANE Select | NP_006199.2:p.Lys606Asn |