HGVS | Genome Assembly |
---|---|
NC_000010.11:g.43077064G>C , CM000672.2:g.43077064G>C | GRCh38 |
NC_000010.10:g.43572512G>C , CM000672.1:g.43572512G>C | GRCh37 |
NC_000010.9:g.42892518G>C | NCBI36 |
NG_007489.1:g.4996G>C , LRG_518:g.4996G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000671844.1:c.-195G>C | ENSP00000500541.1:n.-195G>C | |
ENST00000355710.7:c.-195G>C | ENSP00000347942.3:n.-195G>C | |
XM_011540027.1:c.-195G>C | XP_011538329.1:n.-195G>C | |
NM_020630.5:c.-195G>C | NP_065681.1:n.-195G>C | |
NM_020975.5:c.-195G>C | NP_066124.1:n.-195G>C |