HGVS | Genome Assembly |
---|---|
NC_000015.10:g.97960847G>T , CM000677.2:g.97960847G>T | GRCh38 |
NC_000015.9:g.98504077G>T , CM000677.1:g.98504077G>T | GRCh37 |
NC_000015.8:g.96305081G>T | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000268042.7:c.-15G>T MANE Select | ENSP00000268042.6:n.-15G>T | |
ENST00000268042.6:c.-15G>T | ENSP00000268042.6:n.-15G>T | |
NM_183376.2:c.-15G>T | NP_899232.2:n.-15G>T | |
NM_183376.3:c.-15G>T MANE Select | NP_899232.2:n.-15G>T |