HGVS | Genome Assembly |
---|---|
NC_000011.10:g.2444699G>T , CM000673.2:g.2444699G>T | GRCh38 |
NC_000011.9:g.2465929G>T , CM000673.1:g.2465929G>T | GRCh37 |
NC_000011.8:g.2422505G>T | NCBI36 |
NG_008935.1:g.4709G>T , LRG_287:g.4709G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000496887.7:c.14G>T | ENSP00000434560.2:p.Gly5Val | |
ENST00000496887.6:c.14G>T | ENSP00000434560.1:p.Gly5Val |