Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.63146863T>A , CM000674.2:g.63146863T>A | GRCh38 |
| NC_000012.11:g.63540643T>A , CM000674.1:g.63540643T>A | GRCh37 |
| NC_000012.10:g.61826910T>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000299178.4:c.*496A>T MANE Select | ENSP00000299178.3:n.*496A>T | |
| ENST00000299178.3:c.*496A>T | ENSP00000299178.2:n.*496A>T | |
| ENST00000550940.1:c.538+558A>T | ENSP00000449822.1:n.538+558A>T | |
| NM_000706.4:c.*496A>T | NP_000697.1:n.*496A>T | |
| XM_005269002.3:c.*496A>T | XP_005269059.1:n.*496A>T | |
| NM_000706.5:c.*496A>T MANE Select | NP_000697.1:n.*496A>T |