Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.96617336G= , CM000668.2:g.96617336G= | GRCh38 |
| NC_000006.11:g.97065212G= , CM000668.1:g.97065212G= | GRCh37 |
| NC_000006.10:g.97171933G= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000450218.6:c.*1564G= MANE Select | ENSP00000396390.2:n.*1564G= | |
| XM_006715613.2:c.*1564G= | XP_006715676.1:n.*1564G= | |
| NM_001170807.2:c.*1564G= | NP_001164278.1:n.*1564G= | |
| NM_001322466.1:c.*1564G= | NP_001309395.1:n.*1564G= | |
| NM_001322467.1:c.*1564G= | NP_001309396.1:n.*1564G= | |
| NM_020482.5:c.*1564G= | NP_065228.4:n.*1564G= | |
| NM_001170807.3:c.*1564G= | NP_001164278.1:n.*1564G= | |
| NM_001322466.2:c.*1564G= MANE Select | NP_001309395.1:n.*1564G= | |
| NM_020482.6:c.*1564G= | NP_065228.4:n.*1564G= |