Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.151618123A>T , CM000668.2:g.151618123A>T | GRCh38 |
| NC_000006.11:g.151939258A>T , CM000668.1:g.151939258A>T | GRCh37 |
| NC_000006.10:g.151980951A>T | NCBI36 |
| NG_021198.1:g.129084A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000239374.8:c.2124A>T MANE Select | ENSP00000239374.6:p.Gln708His | |
| ENST00000239374.7:c.2124A>T | ENSP00000239374.6:p.Gln708His | |
| NM_025059.3:c.2124A>T | NP_079335.2:p.Gln708His | |
| XM_011536147.1:c.2142A>T | XP_011534449.1:p.Gln714His | |
| XM_011536148.1:c.1941A>T | XP_011534450.1:p.Gln647His | |
| XM_011536147.2:c.2142A>T | XP_011534449.1:p.Gln714His | |
| XM_011536148.2:c.1941A>T | XP_011534450.1:p.Gln647His | |
| NM_025059.4:c.2124A>T MANE Select | NP_079335.2:p.Gln708His |