HGVS | Genome Assembly |
---|---|
NC_000011.10:g.118312630C= , CM000673.2:g.118312630C= | GRCh38 |
NC_000011.9:g.118183345C= , CM000673.1:g.118183345C= | GRCh37 |
NC_000011.8:g.117688555C= | NCBI36 |
NG_007383.1:g.13051C= , LRG_38:g.13051C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000361763.9:c.116C= MANE Select | ENSP00000354566.4:p.Ser39= | |
ENST00000361763.8:c.116C= | ENSP00000354566.4:p.Ser39= | |
ENST00000526146.5:n.662C= | ||
ENST00000528435.5:n.669C= | ||
ENST00000528600.1:c.98C= | ENSP00000433975.1:p.Ser33= | |
ENST00000529713.5:n.222C= | ||
ENST00000531913.1:n.487C= | ||
NM_000733.3:c.116C= , LRG_38t1:c.116C= | NP_000724.1:p.Ser39= | |
NM_000733.4:c.116C= MANE Select | NP_000724.1:p.Ser39= |