Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.152670531A>T , CM000669.2:g.152670531A>T | GRCh38 |
| NC_000007.13:g.152367616A>T , CM000669.1:g.152367616A>T | GRCh37 |
| NC_000007.12:g.151998549A>T | NCBI36 |
| NG_027988.1:g.10635T>A | |
| NG_027988.2:g.10635T>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_005431.2:c.39+5510T>A MANE Select | NP_005422.1:n.39+5510T>A |
| ENST00000359321.2:c.39+5510T>A MANE Select | ENSP00000352271.1:n.39+5510T>A |
| NM_005431.1:c.39+5510T>A | NP_005422.1:n.39+5510T>A |
| ENST00000359321.1:c.39+5510T>A | ENSP00000352271.1:n.39+5510T>A |
| ENST00000698506.1:c.-48+5510T>A | ENSP00000513758.1:n.-48+5510T>A |
| ENST00000698507.1:n.107+5510T>A |