HGVS | Genome Assembly |
---|---|
NC_000010.11:g.43077059A>T , CM000672.2:g.43077059A>T | GRCh38 |
NC_000010.10:g.43572507A>T , CM000672.1:g.43572507A>T | GRCh37 |
NC_000010.9:g.42892513A>T | NCBI36 |
NG_007489.1:g.4991A>T , LRG_518:g.4991A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000355710.7:c.-200A>T | ENSP00000347942.3:n.-200A>T | |
XM_011540027.1:c.-200A>T | XP_011538329.1:n.-200A>T | |
NM_020630.5:c.-200A>T | NP_065681.1:n.-200A>T | |
NM_020975.5:c.-200A>T | NP_066124.1:n.-200A>T |