Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.32047858C>T , CM000668.2:g.32047858C>T | GRCh38 |
| NC_000006.11:g.32015635C>T , CM000668.1:g.32015635C>T | GRCh37 |
| NC_000006.10:g.32123613C>T | NCBI36 |
| NG_008337.2:g.66517G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001365276.2:c.10200G>A MANE Select | NP_001352205.1:p.Pro3400= |
| ENST00000644971.2:c.10200G>A MANE Select | ENSP00000496448.1:p.Pro3400= |
| NM_001365276.1:c.10200G>A | NP_001352205.1:p.Pro3400= |
| NM_019105.6:c.10194G>A | NP_061978.6:p.Pro3398= |
| NM_019105.7:c.10194G>A | NP_061978.6:p.Pro3398= |
| NM_019105.8:c.10194G>A | NP_061978.6:p.Pro3398= |
| ENST00000375244.7:c.10200G>A | ENSP00000364393.3:p.Pro3400= |
| ENST00000611016.2:c.3354G>A | ENSP00000483409.1:p.Pro1118= |
| ENST00000647633.1:c.10941G>A | ENSP00000497649.1:p.Pro3647= |