Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.5226460A>T , CM000673.2:g.5226460A>T | GRCh38 |
| NC_000011.9:g.5247690A>T , CM000673.1:g.5247690A>T | GRCh37 |
| NC_000011.8:g.5204266A>T | NCBI36 |
| NG_000007.3:g.71156T>A | |
| NG_059281.1:g.5612T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000647020.1:c.315+117T>A | ENSP00000494175.1:n.315+117T>A | |
| ENST00000335295.4:c.315+117T>A MANE Select | ENSP00000333994.3:n.315+117T>A | |
| ENST00000475226.1:n.247+117T>A | ||
| ENST00000485743.1:n.483T>A | ||
| ENST00000633227.1:c.*131+117T>A | ENSP00000488004.1:n.*131+117T>A | |
| NM_000518.4:c.315+117T>A | NP_000509.1:n.315+117T>A | |
| NM_000518.5:c.315+117T>A MANE Select | NP_000509.1:n.315+117T>A |