Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.45988995A>T , CM000683.2:g.45988995A>T | GRCh38 |
| NC_000021.8:g.47408909A>T , CM000683.1:g.47408909A>T | GRCh37 |
| NC_000021.7:g.46233337A>T | NCBI36 |
| NG_008674.1:g.12247A>T , LRG_475:g.12247A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361866.8:c.805-89A>T MANE Select | ENSP00000355180.3:n.805-89A>T | |
| ENST00000361866.7:c.805-89A>T | ENSP00000355180.3:n.805-89A>T | |
| ENST00000612273.1:c.805-89A>T | ENSP00000483630.1:n.805-89A>T | |
| NM_001848.2:c.805-89A>T , LRG_475t1:c.805-89A>T | NP_001839.2:n.805-89A>T | |
| NM_001848.3:c.805-89A>T MANE Select | NP_001839.2:n.805-89A>T |