HGVS | Genome Assembly |
---|---|
NC_000011.10:g.118312676A>T , CM000673.2:g.118312676A>T | GRCh38 |
NC_000011.9:g.118183391A>T , CM000673.1:g.118183391A>T | GRCh37 |
NC_000011.8:g.117688601A>T | NCBI36 |
NG_007383.1:g.13097A>T , LRG_38:g.13097A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000361763.9:c.162A>T MANE Select | ENSP00000354566.4:p.Gly54= | |
ENST00000361763.8:c.162A>T | ENSP00000354566.4:p.Gly54= | |
ENST00000526146.5:n.708A>T | ||
ENST00000528435.5:n.715A>T | ||
ENST00000528600.1:c.144A>T | ENSP00000433975.1:p.Gly48= | |
ENST00000529713.5:n.268A>T | ||
ENST00000531913.1:n.533A>T | ||
NM_000733.3:c.162A>T , LRG_38t1:c.162A>T | NP_000724.1:p.Gly54= | |
NM_000733.4:c.162A>T MANE Select | NP_000724.1:p.Gly54= |