Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.64751596C>G , CM000673.2:g.64751596C>G | GRCh38 |
| NC_000011.9:g.64519068C>G , CM000673.1:g.64519068C>G | GRCh37 |
| NC_000011.8:g.64275644C>G | NCBI36 |
| NG_013018.1:g.14120G>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000164139.4:c.1827+1G>C MANE Select | ENSP00000164139.3:n.1827+1G>C | |
| ENST00000164139.3:c.1827+1G>C | ENSP00000164139.3:n.1827+1G>C | |
| ENST00000377432.7:c.1563+1G>C | ENSP00000366650.3:n.1563+1G>C | |
| ENST00000462303.1:n.151+1G>C | ||
| NM_001164716.1:c.1563+1G>C | NP_001158188.1:n.1563+1G>C | |
| NM_005609.2:c.1827+1G>C | NP_005600.1:n.1827+1G>C | |
| NM_005609.3:c.1827+1G>C | NP_005600.1:n.1827+1G>C | |
| NM_005609.4:c.1827+1G>C MANE Select | NP_005600.1:n.1827+1G>C |