Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.64758244A>G , CM000673.2:g.64758244A>G | GRCh38 |
| NC_000011.9:g.64525716A>G , CM000673.1:g.64525716A>G | GRCh37 |
| NC_000011.8:g.64282292A>G | NCBI36 |
| NG_013018.1:g.7472T>C |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_005609.4:c.528+2T>C MANE Select | NP_005600.1:n.528+2T>C |
| ENST00000164139.4:c.528+2T>C MANE Select | ENSP00000164139.3:n.528+2T>C |
| NM_001164716.1:c.264+2T>C | NP_001158188.1:n.264+2T>C |
| NM_005609.2:c.528+2T>C | NP_005600.1:n.528+2T>C |
| NM_005609.3:c.528+2T>C | NP_005600.1:n.528+2T>C |
| ENST00000164139.3:c.528+2T>C | ENSP00000164139.3:n.528+2T>C |
| ENST00000377432.7:c.264+2T>C | ENSP00000366650.3:n.264+2T>C |