Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.68202881T>A , CM000674.2:g.68202881T>A | GRCh38 |
| NC_000012.11:g.68596661T>A , CM000674.1:g.68596661T>A | GRCh37 |
| NC_000012.10:g.66882928T>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000229134.5:c.364-798A>T MANE Select | ENSP00000229134.4:n.364-798A>T | |
| ENST00000229134.4:c.364-798A>T | ENSP00000229134.4:n.364-798A>T | |
| NM_018402.1:c.364-798A>T | NP_060872.1:n.364-798A>T | |
| XM_011538568.1:c.364-798A>T | XP_011536870.1:n.364-798A>T | |
| XR_945055.1:n.264+4153T>A | ||
| XR_002957418.1:n.280+4153T>A | ||
| NM_018402.2:c.364-798A>T MANE Select | NP_060872.1:n.364-798A>T |