HGVS | Genome Assembly |
---|---|
NC_000011.10:g.118312639G>T , CM000673.2:g.118312639G>T | GRCh38 |
NC_000011.9:g.118183354G>T , CM000673.1:g.118183354G>T | GRCh37 |
NC_000011.8:g.117688564G>T | NCBI36 |
NG_007383.1:g.13060G>T , LRG_38:g.13060G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000361763.9:c.125G>T MANE Select | ENSP00000354566.4:p.Gly42Val | |
ENST00000361763.8:c.125G>T | ENSP00000354566.4:p.Gly42Val | |
ENST00000526146.5:n.671G>T | ||
ENST00000528435.5:n.678G>T | ||
ENST00000528600.1:c.107G>T | ENSP00000433975.1:p.Gly36Val | |
ENST00000529713.5:n.231G>T | ||
ENST00000531913.1:n.496G>T | ||
NM_000733.3:c.125G>T , LRG_38t1:c.125G>T | NP_000724.1:p.Gly42Val | |
NM_000733.4:c.125G>T MANE Select | NP_000724.1:p.Gly42Val |